Search Results - "Davison, E V"
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Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta‐analysis
Published in Ultrasound in obstetrics & gynecology (01-01-2011)“…Objective Array comparative genomic hybridization (CGH) is transforming clinical cytogenetics with its ability to interrogate the human genome at increasingly…”
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Rapid prenatal diagnosis of common trisomies: discordant results between QF-PCR analysis and karyotype analysis on long-term culture for a case of trisomy 18 detected in CVS
Published in Prenatal diagnosis (01-12-2006)“…Objectives QF‐PCR analysis can be used as a rapid test to diagnose primary trisomy in prenatal samples. Mosaicism in CVS detected by QF‐PCR has previously been…”
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Confined placental mosaicism, IUGR, and adverse pregnancy outcome: a controlled retrospective U.K. collaborative survey
Published in Prenatal diagnosis (01-05-1994)“…In a retrospective collaborative study involving 21 U.K. laboratories and 11,775 CVS prenatal diagnostic procedures, a total of 73 cases of confined placental…”
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A further case of confined placental mosaicism for trisomy 2 associated with adverse pregnancy outcome
Published in Prenatal diagnosis (01-07-2003)“…Objectives To add to the knowledge base concerning confined placental mosaicism for trisomy 2. Methods Cytogenetic study of a late CVS referred for…”
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Epidermal mosaicism and Blaschko's lines
Published in Journal of medical genetics (01-09-1993)“…To test the hypothesis that epidermal rather than dermal mosaicism determines Blaschko's lines in hypomelanosis of Ito (HI), we studied the distribution of…”
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First‐trimester prenatal diagnosis of a familial subtelomeric translocation
Published in Ultrasound in obstetrics & gynecology (01-06-2001)“…A new fluorescent in situ hybridization (FISH) technique utilizes a complete set of telomeric probes to screen for deletions or rearrangements within the…”
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STRUCTURAL CHROMOSOME ANOMALIES IN CONGENITAL DIAPHRAGMATIC HERNIA
Published in Prenatal diagnosis (01-11-1996)“…In order to determine the outcome and associated chromosomal and structural anomalies in fetuses diagnosed in utero as having a congenital diaphragmatic…”
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Prenatal diagnosis of mosaicism for partial trisomy 8: a case report including fetal pathology
Published in Prenatal diagnosis (01-10-1999)“…A case of prenatally diagnosed partial trisomy 8 is described. The ‘syndrome’ is associated with skeletal and cardiac anomalies, as well as hepatic…”
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Prospective Prenatal Diagnosis of Prader-Willi Syndrome due to Maternal Disomy for Chromosome 15 following Trisomic Zygote Rescue
Published in Prenatal diagnosis (01-08-1997)“…We present a prenatal predictive diagnosis of Prader–Willi syndrome arising as a result of maternal heterodisomy for chromosome 15. The diagnosis arose…”
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Prenatal testing for uniparental disomy (UPD)
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Cytogenetic analysis of a granulocytic sarcoma in a patient without systemic leukaemia
Published in Journal of clinical pathology (01-01-1991)“…Granulocytic sarcoma is a rare complication of leukaemia. Occasionally it presents before the development of systemic leukaemia when diagnosis may be…”
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Adherence of staphylococcus aureus to influenza A virus-infected Madin-Darby canine kidney cell cultures
Published in Infection and Immunity (01-04-1981)“…Classifications Services IAI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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Meiotic and sperm chromosome analysis in a male carrier of an inverted insertion (3;10)(q13.2;p14p13)
Published in Journal of medical genetics (01-07-1992)“…A phenotypically normal male who fathered a son with the karyotype 46,XY,del(10)(p13) was found to be a balanced carrier of an inverted insertion (3;10)…”
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A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndrome
Published in Journal of medical genetics (01-10-1986)“…A female infant with peripheral pulmonary artery stenosis, growth retardation, and developmental delay was noticed to have facial features consistent with a…”
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Partial trisomy 20p resulting from a recombination of a familial pericentric inversion
Published in Human genetics (01-12-1986)“…Recombination of an inherited pericentric inversion of chromosome 20 has given rise to a child with partial trisomy 20p. To our knowledge no previous familial…”
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Chromosome studies of males in an institution for the mentally handicapped
Published in Journal of medical genetics (01-06-1989)“…Karyotypes were examined in 512 (91.9%) of 557 male patients in an institution for the mentally handicapped. A total of 110 (21.5%) had an abnormal karyotype:…”
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Chromosome 22 abnormalities in Ewing's sarcoma
Published in Journal of clinical pathology (01-08-1989)“…A child with disseminated Ewing's sarcoma underwent cytogenetic investigations which showed different structural rearrangements of chromosome 22 at diagnosis…”
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Partial trisomy 16 as a result of familial 16;20 translocation
Published in Journal of medical genetics (01-10-1984)“…Although trisomy 16 is well recognised in spontaneous abortuses, it is infrequent in livebirths and there is little information about the clinical effects. We…”
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Staphylococcus aureus adherence to influenza A virus-infected and control cell cultures: evidence for multiple adhesins
Published in Proceedings of the Society for Experimental Biology and Medicine (01-01-1986)“…During major epidemics with influenza, there is an increased number of pneumonias due to Staphylococcus aureus with a subsequent high mortality rate. We have…”
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Fibrinogen-mediated adherence of group A Streptococcus to influenza A virus-infected cell cultures
Published in Infection and Immunity (01-11-1982)“…Classifications Services IAI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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