Literature DB >> 5096544

49,XXXXY chromossomal anomaly in a neonate.

A Hayek, V Riccardi, L Atkins, H Hendren.   

Abstract

Entities:  

Mesh:

Year:  1971        PMID: 5096544      PMCID: PMC1469009          DOI: 10.1136/jmg.8.2.220

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


× No keyword cloud information.
  3 in total

1.  A child with 49 chromosomes.

Authors:  M FRACCARO; K KAIJSER; J LINDSTEN
Journal:  Lancet       Date:  1960-10-22       Impact factor: 79.321

2.  [Gonadosomal dysgenesia with 49 chromosomes].

Authors:  A Bitan; P Schaefer; C Bach
Journal:  Ann Pediatr (Paris)       Date:  1969-12-02

3.  XXXXY boy. A 15-month-old child with normal intellectual development.

Authors:  L R Shapiro; L Y Hsu; M E Calvin; K Hirschhorn
Journal:  Am J Dis Child       Date:  1970-01
  3 in total
  3 in total

1.  The influence of inactive chromosomes on human development. Anomalous sex chromosome complements and the phenotype.

Authors:  P Barlow
Journal:  Humangenetik       Date:  1973

2.  49,XXXXY: a distinct phenotype. Three new cases and review.

Authors:  J Peet; D D Weaver; G H Vance
Journal:  J Med Genet       Date:  1998-05       Impact factor: 6.318

3.  Epiphysial dysplasia: a constant finding in the XXXXY syndrome.

Authors:  R Schmidt; M Pajewski; M Rosenblatt
Journal:  J Med Genet       Date:  1978-08       Impact factor: 6.318

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.