Literature DB >> 7159717

A cytogenetic survey of 14,069 newborn infants. IV. Further follow-up on the children with sex chromosome anomalies.

J A Evans, R de von Flindt, C Greenberg, S Ramsay, J L Hamerton.   

Abstract

Between 1970 and 1973, 14,069 consecutive liveborn infants at the Women's Centre, Winnipeg, were subjected to karyotypic analysis. The details of the materials and methods and the preliminary findings of the study have been previously published [1,2]. A total of 15 nonmosaic and 4 mosaic infants with sex chromosome anomalies were detected: 12 males and 7 females. These children have been followed wherever possible by physical and developmental evaluations, and preliminary findings have been reported previously [3]. In order to obtain further baseline data on these children while they were still prepubertal, it was decided to recontact all families and encourage them to present their children for further physical evaluation and psychologic testing. Details of these investigations and their results are given in this paper.

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Year:  1982        PMID: 7159717

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


  4 in total

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Journal:  Eur J Hum Genet       Date:  2009-07-01       Impact factor: 4.246

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Journal:  Acta Paediatr       Date:  2011-04-08       Impact factor: 2.299

Review 3.  The spectrum of the behavioral phenotype in boys and adolescents 47,XXY (Klinefelter syndrome).

Authors:  Nicole Tartaglia; Lisa Cordeiro; Susan Howell; Rebecca Wilson; Jennifer Janusz
Journal:  Pediatr Endocrinol Rev       Date:  2010-12

4.  Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis.

Authors:  Xin-Yan Lu; Mai T Phung; Chad A Shaw; Kim Pham; Sarah E Neil; Ankita Patel; Trilochan Sahoo; Carlos A Bacino; Pawel Stankiewicz; Sung-Hae Lee Kang; Seema Lalani; A Craig Chinault; James R Lupski; Sau W Cheung; Arthur L Beaudet
Journal:  Pediatrics       Date:  2008-12       Impact factor: 7.124

  4 in total

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