Usefulness of early morphological ultrasound in association with cell-free DNA testing in case of atypical serum markers in first trimester of pregnancy: A retrospective study over 5 years
Early morphologic ultrasound, generally carried out in case of atypical first trimester serum markers (PAPP-A and/or free hCGβ <0.30 MoM), has not been re-evaluated since the possibility of performing a cell-free fetal DNA analysis in this indication. Our objective was to evaluate the usefulness...
Saved in:
Published in: | Journal of gynecology obstetrics and human reproduction Vol. 53; no. 4; p. 102745 |
---|---|
Main Authors: | , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
France
Elsevier Masson SAS
01-04-2024
|
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Abstract | Early morphologic ultrasound, generally carried out in case of atypical first trimester serum markers (PAPP-A and/or free hCGβ <0.30 MoM), has not been re-evaluated since the possibility of performing a cell-free fetal DNA analysis in this indication. Our objective was to evaluate the usefulness of early morphological ultrasound in case of atypical profile of serum markers performed in association with Non-Invasive Prenatal Testing (NIPT).
This was a single-center retrospective study in a tertiary maternity. Between January 2017 and December 2021, women with an atypical first trimester serum markers and low/intermediate risk for trisomy 21 (<1/50) were included. The clinical data, results of first trimester serum markers, NIPT, early morphological ultrasound and subsequent ultrasounds and other investigations (amniocentesis, pregnancy outcomes) were analyzed.
After exclusion of women with high-risk of trisomy 21 and lost to follow-up, 163 women were included. In 72 % of cases (117/163), women had a low risk of trisomy 21, and 39 % (59/163) had an early morphological ultrasound. Early morphological ultrasound was useful to detect severe IUGR leading to the suspicion of triploidy (3/163, 1.8 %). In all other situations, it did not allow earlier management. After analysis of the 3 triploidy cases, a collapsed profile for both serum markers was demonstrated (<0.25 MoM).
Systematic early morphological ultrasound in case of an atypical serum marker profile seems useless considering the performance of NIPT. An ultrasound restricted to women with both markers below 0.25 MoM would allow the early detection of triploidy. |
---|---|
AbstractList | Early morphologic ultrasound, generally carried out in case of atypical first trimester serum markers (PAPP-A and/or free hCGβ <0.30 MoM), has not been re-evaluated since the possibility of performing a cell-free fetal DNA analysis in this indication. Our objective was to evaluate the usefulness of early morphological ultrasound in case of atypical profile of serum markers performed in association with Non-Invasive Prenatal Testing (NIPT).
This was a single-center retrospective study in a tertiary maternity. Between January 2017 and December 2021, women with an atypical first trimester serum markers and low/intermediate risk for trisomy 21 (<1/50) were included. The clinical data, results of first trimester serum markers, NIPT, early morphological ultrasound and subsequent ultrasounds and other investigations (amniocentesis, pregnancy outcomes) were analyzed.
After exclusion of women with high-risk of trisomy 21 and lost to follow-up, 163 women were included. In 72 % of cases (117/163), women had a low risk of trisomy 21, and 39 % (59/163) had an early morphological ultrasound. Early morphological ultrasound was useful to detect severe IUGR leading to the suspicion of triploidy (3/163, 1.8 %). In all other situations, it did not allow earlier management. After analysis of the 3 triploidy cases, a collapsed profile for both serum markers was demonstrated (<0.25 MoM).
Systematic early morphological ultrasound in case of an atypical serum marker profile seems useless considering the performance of NIPT. An ultrasound restricted to women with both markers below 0.25 MoM would allow the early detection of triploidy. BACKGROUNDEarly morphologic ultrasound, generally carried out in case of atypical first trimester serum markers (PAPP-A and/or free hCGβ <0.30 MoM), has not been re-evaluated since the possibility of performing a cell-free fetal DNA analysis in this indication. Our objective was to evaluate the usefulness of early morphological ultrasound in case of atypical profile of serum markers performed in association with Non-Invasive Prenatal Testing (NIPT).METHODSThis was a single-center retrospective study in a tertiary maternity. Between January 2017 and December 2021, women with an atypical first trimester serum markers and low/intermediate risk for trisomy 21 (<1/50) were included. The clinical data, results of first trimester serum markers, NIPT, early morphological ultrasound and subsequent ultrasounds and other investigations (amniocentesis, pregnancy outcomes) were analyzed.RESULTSAfter exclusion of women with high-risk of trisomy 21 and lost to follow-up, 163 women were included. In 72 % of cases (117/163), women had a low risk of trisomy 21, and 39 % (59/163) had an early morphological ultrasound. Early morphological ultrasound was useful to detect severe IUGR leading to the suspicion of triploidy (3/163, 1.8 %). In all other situations, it did not allow earlier management. After analysis of the 3 triploidy cases, a collapsed profile for both serum markers was demonstrated (<0.25 MoM).CONCLUSIONSSystematic early morphological ultrasound in case of an atypical serum marker profile seems useless considering the performance of NIPT. An ultrasound restricted to women with both markers below 0.25 MoM would allow the early detection of triploidy. |
ArticleNumber | 102745 |
Author | Anselem, Olivia Jordan, Pénélope Khattabi, Laila El Buron-Fouque, Charlotte Laguillier-Morizot, Christelle Claudel, Noémie Tsatsaris, Vassilis Guibourdenche, Jean Athiel, Yoann |
Author_xml | – sequence: 1 givenname: Noémie surname: Claudel fullname: Claudel, Noémie organization: Maternité Port-Royal, Groupe hospitalier Cochin Broca Hôtel-Dieu, Assistance Publique-Hôpitaux de Paris, Paris, 75014, France – sequence: 2 givenname: Olivia surname: Anselem fullname: Anselem, Olivia organization: Maternité Port-Royal, Groupe hospitalier Cochin Broca Hôtel-Dieu, Assistance Publique-Hôpitaux de Paris, Paris, 75014, France – sequence: 3 givenname: Charlotte surname: Buron-Fouque fullname: Buron-Fouque, Charlotte organization: Maternité Port-Royal, Groupe hospitalier Cochin Broca Hôtel-Dieu, Assistance Publique-Hôpitaux de Paris, Paris, 75014, France – sequence: 4 givenname: Laila El surname: Khattabi fullname: Khattabi, Laila El organization: NIPT plateform, Department of Cytogenetics, AP-HP, Hôpital Cochin, Paris, France – sequence: 5 givenname: Christelle surname: Laguillier-Morizot fullname: Laguillier-Morizot, Christelle organization: Université Paris Cité, Paris, France – sequence: 6 givenname: Pénélope surname: Jordan fullname: Jordan, Pénélope organization: NIPT plateform, Department of Cytogenetics, AP-HP, Hôpital Cochin, Paris, France – sequence: 7 givenname: Vassilis surname: Tsatsaris fullname: Tsatsaris, Vassilis organization: Maternité Port-Royal, Groupe hospitalier Cochin Broca Hôtel-Dieu, Assistance Publique-Hôpitaux de Paris, Paris, 75014, France – sequence: 8 givenname: Jean surname: Guibourdenche fullname: Guibourdenche, Jean organization: Université Paris Cité, Paris, France – sequence: 9 givenname: Yoann surname: Athiel fullname: Athiel, Yoann email: yoann.athiel@aphp.fr organization: Maternité Port-Royal, Groupe hospitalier Cochin Broca Hôtel-Dieu, Assistance Publique-Hôpitaux de Paris, Paris, 75014, France |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38367703$$D View this record in MEDLINE/PubMed |
BookMark | eNp9kc1u1DAUhS1UREvpEyAhL9lk8E8m9iCxGJVfqYINXVuuczPjIbGDrzNV3o2Hw-kUxIqVLd_vnHuvz3NyFmIAQl5ytuKMN28Oq0Pcxf1KMFGXF6Hq9RNyIepGV0rX6uyf-zm5QjwwxrgWTSObZ-RcatkoxeQF-XWL0E19AEQaOwo29TMdYhr3sY8772xPpz4ni3EKLfWBWsTovM0-Bnrv85466PuqSwD0_dctzYDZh91COouweNo8jw9GCGka6GDTD0i4EJ1PmGlOfigqSAs8JtgFG9z8lm5pgpwijuCyPwLFPLUzjccCrulcJsUX5Glne4Srx_OS3H788P36c3Xz7dOX6-1N5STb5EoLxi2TVm0aK2WnYdN2XDdCacEbt1EAmjsmW7CiXreuLRVrdcesvGsZV0Jektcn3zHFn1OZ1Qwel71tgDihERuhxZpzoQoqT6grk2OCzoxlPZtmw5lZkjMH85CcWZIzp-SK6tVjg-lugPav5k9OBXh3AqCsefSQDDoPwUHrU_ke00b_3wa_ASa6sKo |
Cites_doi | 10.1002/pd.2505 10.3390/ijms24087669 10.1186/s12967-019-02152-7 10.1016/j.jgyn.2014.05.012 |
ContentType | Journal Article |
Copyright | 2024 Elsevier Masson SAS Copyright © 2024. Published by Elsevier Masson SAS. |
Copyright_xml | – notice: 2024 Elsevier Masson SAS – notice: Copyright © 2024. Published by Elsevier Masson SAS. |
DBID | NPM AAYXX CITATION 7X8 |
DOI | 10.1016/j.jogoh.2024.102745 |
DatabaseName | PubMed CrossRef MEDLINE - Academic |
DatabaseTitle | PubMed CrossRef MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic PubMed |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 2468-7847 |
EndPage | 102745 |
ExternalDocumentID | 10_1016_j_jogoh_2024_102745 38367703 S2468784724000242 |
Genre | Journal Article |
GroupedDBID | 0R~ AACTN AAEDT AAEDW AAIAV AAKOC AALRI AAQFI AAXUO ABMAC ACDAQ ACGFS ACRLP AEBSH AFTJW AFXIZ AGUBO AIEXJ AIKHN AITUG ALMA_UNASSIGNED_HOLDINGS AMRAJ AXJTR BNPGV EFJIC FDB FIRID KOM O9- ROL SPCBC SSH SSZ T5K ~G- 53G AFJKZ NPM AAYXX CITATION 7X8 |
ID | FETCH-LOGICAL-c309t-8201a03a796a33f8e9df186278216c97ee81c03dea245dcd627aa8f0a3bd01723 |
ISSN | 2468-7847 |
IngestDate | Sat Oct 26 05:54:24 EDT 2024 Thu Sep 26 16:15:26 EDT 2024 Sat Nov 02 12:30:51 EDT 2024 Sat Apr 13 16:39:07 EDT 2024 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 4 |
Keywords | ACLF Aneuploidy MoM Early morphological fetal ultrasound CFDT Decreased serum markers WG T21 Prenatal diagnosis TOP IUGR T13 T16 T18 NIPT Triploidy aneuploidy early morphological fetal ultrasound decreased serum markers prenatal diagnosis triploidy |
Language | English |
License | Copyright © 2024. Published by Elsevier Masson SAS. |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c309t-8201a03a796a33f8e9df186278216c97ee81c03dea245dcd627aa8f0a3bd01723 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
PMID | 38367703 |
PQID | 2928251127 |
PQPubID | 23479 |
PageCount | 1 |
ParticipantIDs | proquest_miscellaneous_2928251127 crossref_primary_10_1016_j_jogoh_2024_102745 pubmed_primary_38367703 elsevier_sciencedirect_doi_10_1016_j_jogoh_2024_102745 |
PublicationCentury | 2000 |
PublicationDate | 2024-04-01 |
PublicationDateYYYYMMDD | 2024-04-01 |
PublicationDate_xml | – month: 04 year: 2024 text: 2024-04-01 day: 01 |
PublicationDecade | 2020 |
PublicationPlace | France |
PublicationPlace_xml | – name: France |
PublicationTitle | Journal of gynecology obstetrics and human reproduction |
PublicationTitleAlternate | J Gynecol Obstet Hum Reprod |
PublicationYear | 2024 |
Publisher | Elsevier Masson SAS |
Publisher_xml | – name: Elsevier Masson SAS |
References | Guibourdenche, Leguy, Pidoux, Hebert-Schuster, Laguillier, Anselem (bib0009) 2023; 24 Eftekhariyazdi, Khaligh, Suizi, Naghibi Nasab, Zare-Abdollahi (bib0013) 2019; 11 Valérie (bib0001) 2017 Benachi, Letourneau, Kleinfinger, Senat, Gautier, Favre (bib0005) 2016; 45 . Huang, Hoffman, Meschino, Kingdom, Okun (bib0008) 2010; 30 Pan, Yang, He, Han, Zhen, Yang (bib0014) 2021; 34 Carrara, Vivanti, Jani, Demain, Costa, Benachi (bib0006) 2019; 17 Muller, Dreux, Czerkiewicz, Bernard, Guibourdenche, Lacroix (bib0002) 2014; 43 ACLF. Guide des bonnes pratiques en cytogénétique 2020. [consulté le 9 aout 2022]. Disponible (bib0004) 2019 Harraway (bib0011) 2017; 46 Orphanet. Triploïdie. [consulté le 9 aout 2022]. Disponible Cuckle, Arbuzova, Spencer, Crossley, Barkai, Krantz (bib0010) 2003; 23 Gagnon, Wilson (bib0003) 2008; 30 Pan (10.1016/j.jogoh.2024.102745_bib0014) 2021; 34 Guibourdenche (10.1016/j.jogoh.2024.102745_bib0009) 2023; 24 Gagnon (10.1016/j.jogoh.2024.102745_bib0003) 2008; 30 10.1016/j.jogoh.2024.102745_bib0012 Harraway (10.1016/j.jogoh.2024.102745_bib0011) 2017; 46 Huang (10.1016/j.jogoh.2024.102745_bib0008) 2010; 30 Benachi (10.1016/j.jogoh.2024.102745_bib0005) 2016; 45 Carrara (10.1016/j.jogoh.2024.102745_bib0006) 2019; 17 Valérie (10.1016/j.jogoh.2024.102745_bib0001) 2017 Eftekhariyazdi (10.1016/j.jogoh.2024.102745_bib0013) 2019; 11 Cuckle (10.1016/j.jogoh.2024.102745_bib0010) 2003; 23 (10.1016/j.jogoh.2024.102745_bib0004) 2019 Muller (10.1016/j.jogoh.2024.102745_bib0002) 2014; 43 10.1016/j.jogoh.2024.102745_bib0007 |
References_xml | – start-page: 11 year: 2017 ident: bib0001 article-title: HAS publication-title: Place des test ADN libre circulant dans le sang maternel dans le dépistage de la trisomie 21 foetale contributor: fullname: Valérie – volume: 43 start-page: 671 year: 2014 end-page: 679 ident: bib0002 article-title: Dépistage de la trisomie 21 par les marqueurs sériques maternels : justification des commentaires appliqués par les biologistes publication-title: J Gynécologie Obstétrique Biol Reprod contributor: fullname: Lacroix – volume: 23 start-page: 385‑8 year: 2003 ident: bib0010 article-title: Frequency and clinical consequences of extremely high maternal serum PAPP-A levels publication-title: Prenat Diagn. mai contributor: fullname: Krantz – year: 2019 ident: bib0004 article-title: Recommandations pour le depistage des anomalies chromosomiques fœtales par l'etude de l'ADN libre circulant (ADNlc) – volume: 45 start-page: 633‑40 year: 2016 ident: bib0005 article-title: [Performance and indications of noninvasive prenatal testing using cell free circulating fetal DNA (cffDNA) for the detection of fetal trisomy 21, 18 and 13 in France] publication-title: J Gynecol Obstet Biol Reprod (Paris) contributor: fullname: Favre – volume: 24 start-page: 7669 year: 2023 ident: bib0009 article-title: Biochemical screening for fetal trisomy 21: pathophysiology of maternal serum markers and involvement of the placenta publication-title: Int J Mol Sci. janv contributor: fullname: Anselem – volume: 30 start-page: 918‑32 year: 2008 ident: bib0003 article-title: Society of obstetricians and gynaecologists of Canada genetics committee. Obstetrical complications associated with abnormal maternal serum markers analytes publication-title: J Obstet Gynaecol Can JOGC J Obstet Gynecol Can JOGC contributor: fullname: Wilson – volume: 11 start-page: 124‑6 year: 2019 ident: bib0013 article-title: Triploidy and routine combined first trimester pregnancy screening publication-title: Avicenna J Med Biotechnol. mars contributor: fullname: Zare-Abdollahi – volume: 46 start-page: 735‑9 year: 2017 ident: bib0011 article-title: Non-invasive prenatal testing publication-title: Aust Fam Physician contributor: fullname: Harraway – volume: 34 start-page: 4072‑6 year: 2021 ident: bib0014 article-title: Early prenatal detection of triploidy: a 9-year experience in mainland China publication-title: J Matern-Fetal Neonatal Med Off J Eur Assoc Perinat Med Fed Asia Ocean Perinat Soc Int Soc Perinat Obstet. déc contributor: fullname: Yang – volume: 17 start-page: 398 year: 2019 ident: bib0006 article-title: Usefulness and reliability of cell free fetal DNA screening for main trisomies in case of atypical profile on first trimester maternal serum screening publication-title: J Transl Med contributor: fullname: Benachi – volume: 30 start-page: 471‑7 year: 2010 ident: bib0008 article-title: Prediction of adverse pregnancy outcomes by combinations of first and second trimester biochemistry markers used in the routine prenatal screening of Down syndrome publication-title: Prenat Diagn contributor: fullname: Okun – volume: 30 start-page: 471‑7 issue: 5 year: 2010 ident: 10.1016/j.jogoh.2024.102745_bib0008 article-title: Prediction of adverse pregnancy outcomes by combinations of first and second trimester biochemistry markers used in the routine prenatal screening of Down syndrome publication-title: Prenat Diagn doi: 10.1002/pd.2505 contributor: fullname: Huang – volume: 34 start-page: 4072‑6 issue: 24 year: 2021 ident: 10.1016/j.jogoh.2024.102745_bib0014 article-title: Early prenatal detection of triploidy: a 9-year experience in mainland China publication-title: J Matern-Fetal Neonatal Med Off J Eur Assoc Perinat Med Fed Asia Ocean Perinat Soc Int Soc Perinat Obstet. déc contributor: fullname: Pan – start-page: 11 year: 2017 ident: 10.1016/j.jogoh.2024.102745_bib0001 article-title: HAS contributor: fullname: Valérie – volume: 24 start-page: 7669 issue: 8 year: 2023 ident: 10.1016/j.jogoh.2024.102745_bib0009 article-title: Biochemical screening for fetal trisomy 21: pathophysiology of maternal serum markers and involvement of the placenta publication-title: Int J Mol Sci. janv doi: 10.3390/ijms24087669 contributor: fullname: Guibourdenche – year: 2019 ident: 10.1016/j.jogoh.2024.102745_bib0004 – ident: 10.1016/j.jogoh.2024.102745_bib0007 – ident: 10.1016/j.jogoh.2024.102745_bib0012 – volume: 11 start-page: 124‑6 issue: 1 year: 2019 ident: 10.1016/j.jogoh.2024.102745_bib0013 article-title: Triploidy and routine combined first trimester pregnancy screening publication-title: Avicenna J Med Biotechnol. mars contributor: fullname: Eftekhariyazdi – volume: 17 start-page: 398 issue: 1 year: 2019 ident: 10.1016/j.jogoh.2024.102745_bib0006 article-title: Usefulness and reliability of cell free fetal DNA screening for main trisomies in case of atypical profile on first trimester maternal serum screening publication-title: J Transl Med doi: 10.1186/s12967-019-02152-7 contributor: fullname: Carrara – volume: 30 start-page: 918‑32 issue: 10 year: 2008 ident: 10.1016/j.jogoh.2024.102745_bib0003 article-title: Society of obstetricians and gynaecologists of Canada genetics committee. Obstetrical complications associated with abnormal maternal serum markers analytes publication-title: J Obstet Gynaecol Can JOGC J Obstet Gynecol Can JOGC contributor: fullname: Gagnon – volume: 23 start-page: 385‑8 issue: 5 year: 2003 ident: 10.1016/j.jogoh.2024.102745_bib0010 article-title: Frequency and clinical consequences of extremely high maternal serum PAPP-A levels publication-title: Prenat Diagn. mai contributor: fullname: Cuckle – volume: 45 start-page: 633‑40 issue: 6 year: 2016 ident: 10.1016/j.jogoh.2024.102745_bib0005 article-title: [Performance and indications of noninvasive prenatal testing using cell free circulating fetal DNA (cffDNA) for the detection of fetal trisomy 21, 18 and 13 in France] publication-title: J Gynecol Obstet Biol Reprod (Paris) contributor: fullname: Benachi – volume: 43 start-page: 671 issue: 9 year: 2014 ident: 10.1016/j.jogoh.2024.102745_bib0002 article-title: Dépistage de la trisomie 21 par les marqueurs sériques maternels : justification des commentaires appliqués par les biologistes publication-title: J Gynécologie Obstétrique Biol Reprod doi: 10.1016/j.jgyn.2014.05.012 contributor: fullname: Muller – volume: 46 start-page: 735‑9 issue: 10 year: 2017 ident: 10.1016/j.jogoh.2024.102745_bib0011 article-title: Non-invasive prenatal testing publication-title: Aust Fam Physician contributor: fullname: Harraway |
SSID | ssj0001826636 |
Score | 2.3037772 |
Snippet | Early morphologic ultrasound, generally carried out in case of atypical first trimester serum markers (PAPP-A and/or free hCGβ <0.30 MoM), has not been... BACKGROUNDEarly morphologic ultrasound, generally carried out in case of atypical first trimester serum markers (PAPP-A and/or free hCGβ <0.30 MoM), has not... |
SourceID | proquest crossref pubmed elsevier |
SourceType | Aggregation Database Index Database Publisher |
StartPage | 102745 |
SubjectTerms | Aneuploidy Decreased serum markers Early morphological fetal ultrasound NIPT Prenatal diagnosis Triploidy |
Title | Usefulness of early morphological ultrasound in association with cell-free DNA testing in case of atypical serum markers in first trimester of pregnancy: A retrospective study over 5 years |
URI | https://dx.doi.org/10.1016/j.jogoh.2024.102745 https://www.ncbi.nlm.nih.gov/pubmed/38367703 https://search.proquest.com/docview/2928251127 |
Volume | 53 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1ba9swFBZtCmMvY_dlNzTYm-fi-2VvoU3ZBs0e0kLfjGJLqYNjFcce5L_tx-0cyZd0a8Y22IsJimIZn0_S0cl3vkPI-wzOscJPM5MHIjQ9N7WQBBCYqW1lfgonktRWRWzn4ewqOp1604PDrsDi0PZfLQ1tYGvMnP0La_c3hQb4DDaHK1gdrn9k98sNF02hFjDwA7nSL15LeJv9KtcUdcU2WE4Jgx1ssE_LQ-dFYYqKc-N0NjFqVOHQaS8p03F_Vm9vdDIlr5q1sUaCT6VotSIHX9KosWIA6i8oNnXFl6jpsdUp8BWvK9lld2ptWwNJpIZvbOFZN3t85eW25KlWi5ILuDWWFdDi0rrGIEpzKuXaHVbBScGaTHMQZlLzAdb5AHDMxOdqMnwt8m_5EJdoKlmaZ7KBDbPnI8iOD4Vb0zWra7Zos8rzghnTYjd24uxSblRAr0vqOcd3DcvpZD4svw7mpIWR1gM95ne0tfuHFjtu54l357akIySr45VcSvwHzPFQMiPUQpo_6X3PcRAcA9m96EEdkiMHVlF_RI4mn6dXX4YQIhwNA1UEs3-uTldLMRh_GW2f77XvbKV8rIuH5EFrcDrRqH5EDnj5mNw7b-kfT8j3AdxUCqrATW-Bmw7gpnlJd8BNEdy0BzcFcNMW3NgTwY337MBNFbhpC27socBNe3Bj5x7cH-mE3oI2VdCmCG3qUwXtp-TybHpx8slsy4-YqWvFtYm-MbNcFsYBc10R8TgTdhQ44FPbQRqHnEd2arkZZ47nZ2kG3zAWCYu5iwwjK-4zMiplyV8QKuw0EFa0iITreZ4lItg2F0LEPgtZDF7qmHzoDJPcaJWZpKNfrhJlxwTtmGg7jknQGS9pHWXtACcAuN__8F1n6gS2EXznrOSy2SROrJLYbScck-caA_2TuJEbhOAZvPzXYV-R-8Pse01GddXwN-RwkzVvW0z_AG6DAEA |
link.rule.ids | 315,782,786,27935,27936 |
linkProvider | Elsevier |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Usefulness+of+early+morphological+ultrasound+in+association+with+cell-free+DNA+testing+in+case+of+atypical+serum+markers+in+first+trimester+of+pregnancy%3A+A+retrospective+study+over+5+years&rft.jtitle=Journal+of+gynecology+obstetrics+and+human+reproduction&rft.au=Claudel%2C+No%C3%A9mie&rft.au=Anselem%2C+Olivia&rft.au=Buron-Fouque%2C+Charlotte&rft.au=Khattabi%2C+Laila+El&rft.date=2024-04-01&rft.pub=Elsevier+Masson+SAS&rft.issn=2468-7847&rft.eissn=2468-7847&rft.volume=53&rft.issue=4&rft_id=info:doi/10.1016%2Fj.jogoh.2024.102745&rft.externalDocID=S2468784724000242 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2468-7847&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2468-7847&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2468-7847&client=summon |