Prenatal Diagnosis of Digeorge Syndrome

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Published in:	Taiwanese journal of obstetrics & gynecology Vol. 47; no. 4; pp. 441 - 442
Main Authors:	Göktolga, Ümit, Gezginç, Kazim, Ceyhan, S. Temel, Fidan, Ulaş, Ergün, Ali, Bahçe, Muhterem, Başer, Iskender
Format:	Journal Article
Language:	English
Published:	Elsevier B.V 01-12-2008 Elsevier
Subjects:	Internal Medicine Obstetrics and Gynecology
Online Access:	Get full text
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Author	Bahçe, Muhterem Fidan, Ulaş Göktolga, Ümit Ceyhan, S. Temel Gezginç, Kazim Ergün, Ali Başer, Iskender
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References	Oh, Min, Lee (bib1) 2002; 17 Lim, Han, Jun (bib7) 2000; 43 Driscoll, Budarf, Emanuel (bib3) 1991; 338 Perez, Sullivan (bib5) 2002; 14 Driscoll, Salvin, Sellinger, Budarf, McDonaldMcGinn, Zackai, Emanuel (bib2) 1993; 30 Goldmuntz, Driscoll, Budarf, Zackai, McDonald-McGinn, Biegel, Emanuel (bib8) 1993; 30 Motzkin, Marion, Goldberg, Shprintzen, Saenger (bib4) 1993; 123 Maeda, Yamagishi, Matsuoka (bib9) 2000; 92 Yamagishi, Srivastava (bib6) 2003; 9 Motzkin (10.1016/S1028-4559(09)60014-0_bib4) 1993; 123 Lim (10.1016/S1028-4559(09)60014-0_bib7) 2000; 43 Driscoll (10.1016/S1028-4559(09)60014-0_bib3) 1991; 338 Driscoll (10.1016/S1028-4559(09)60014-0_bib2) 1993; 30 Oh (10.1016/S1028-4559(09)60014-0_bib1) 2002; 17 Perez (10.1016/S1028-4559(09)60014-0_bib5) 2002; 14 Goldmuntz (10.1016/S1028-4559(09)60014-0_bib8) 1993; 30 Yamagishi (10.1016/S1028-4559(09)60014-0_bib6) 2003; 9 Maeda (10.1016/S1028-4559(09)60014-0_bib9) 2000; 92
References_xml	– volume: 43 start-page: 1147 year: 2000 end-page: 1153 ident: bib7 article-title: Clinical application of preimplantation genetic diagnosis (PGD) using fluorescence publication-title: Korean J Obstet Gynecol contributor: fullname: Jun – volume: 123 start-page: 406 year: 1993 end-page: 410 ident: bib4 article-title: Variable phenotypes in velocardiofacial syndrome with chromosomal deletion publication-title: J Pediatr contributor: fullname: Saenger – volume: 14 start-page: 678 year: 2002 end-page: 683 ident: bib5 article-title: Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes) publication-title: Curr Opin Pediatr contributor: fullname: Sullivan – volume: 30 start-page: 813 year: 1993 end-page: 817 ident: bib2 article-title: Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis publication-title: J Med Genet contributor: fullname: Emanuel – volume: 9 start-page: 383 year: 2003 end-page: 389 ident: bib6 article-title: Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome publication-title: Trends Mol Med contributor: fullname: Srivastava – volume: 30 start-page: 807 year: 1993 end-page: 812 ident: bib8 article-title: Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects publication-title: J Med Genet contributor: fullname: Emanuel – volume: 338 start-page: 1390 year: 1991 end-page: 1391 ident: bib3 article-title: Antenatal diagnosis of DiGeorge syndrome publication-title: Lancet contributor: fullname: Emanuel – volume: 17 start-page: 125 year: 2002 end-page: 128 ident: bib1 article-title: Prenatal diagnosis of tetralogy of Fallot associated with chromosome 22q11 deletion publication-title: J Korean Med Sci contributor: fullname: Lee – volume: 92 start-page: 269 year: 2000 end-page: 272 ident: bib9 article-title: Frequent association of 22q11.2 deletion with tetralogy of Fallot publication-title: Am J Med Genet contributor: fullname: Matsuoka – volume: 9 start-page: 383 year: 2003 ident: 10.1016/S1028-4559(09)60014-0_bib6 article-title: Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome publication-title: Trends Mol Med doi: 10.1016/S1471-4914(03)00141-2 contributor: fullname: Yamagishi – volume: 17 start-page: 125 year: 2002 ident: 10.1016/S1028-4559(09)60014-0_bib1 article-title: Prenatal diagnosis of tetralogy of Fallot associated with chromosome 22q11 deletion publication-title: J Korean Med Sci doi: 10.3346/jkms.2002.17.1.125 contributor: fullname: Oh – volume: 43 start-page: 1147 year: 2000 ident: 10.1016/S1028-4559(09)60014-0_bib7 article-title: Clinical application of preimplantation genetic diagnosis (PGD) using fluorescence in situ hybridization to balanced reciprocal or Robertsonian translocation carriers in human IVF-ET program publication-title: Korean J Obstet Gynecol contributor: fullname: Lim – volume: 14 start-page: 678 year: 2002 ident: 10.1016/S1028-4559(09)60014-0_bib5 article-title: Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes) publication-title: Curr Opin Pediatr doi: 10.1097/00008480-200212000-00005 contributor: fullname: Perez – volume: 92 start-page: 269 year: 2000 ident: 10.1016/S1028-4559(09)60014-0_bib9 article-title: Frequent association of 22q11.2 deletion with tetralogy of Fallot publication-title: Am J Med Genet doi: 10.1002/(SICI)1096-8628(20000605)92:4<269::AID-AJMG9>3.0.CO;2-L contributor: fullname: Maeda – volume: 30 start-page: 813 year: 1993 ident: 10.1016/S1028-4559(09)60014-0_bib2 article-title: Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis publication-title: J Med Genet doi: 10.1136/jmg.30.10.813 contributor: fullname: Driscoll – volume: 123 start-page: 406 year: 1993 ident: 10.1016/S1028-4559(09)60014-0_bib4 article-title: Variable phenotypes in velocardiofacial syndrome with chromosomal deletion publication-title: J Pediatr doi: 10.1016/S0022-3476(05)81740-8 contributor: fullname: Motzkin – volume: 30 start-page: 807 year: 1993 ident: 10.1016/S1028-4559(09)60014-0_bib8 article-title: Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects publication-title: J Med Genet doi: 10.1136/jmg.30.10.807 contributor: fullname: Goldmuntz – volume: 338 start-page: 1390 year: 1991 ident: 10.1016/S1028-4559(09)60014-0_bib3 article-title: Antenatal diagnosis of DiGeorge syndrome publication-title: Lancet doi: 10.1016/0140-6736(91)92264-3 contributor: fullname: Driscoll
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Title	Prenatal Diagnosis of Digeorge Syndrome
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