Literature DB >> 14283740

A PATIENT WITH 48 CHROMOSOMES (XYYY).

P L TOWNES, N A ZIEGLER, L W LENHARD.   

Abstract

Entities:  

Keywords:  CHILD; CHROMOSOME ABNORMALITIES; CLASSIFICATION; DIAGNOSIS; GENETICS, HUMAN

Mesh:

Year:  1965        PMID: 14283740     DOI: 10.1016/s0140-6736(65)91315-2

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


× No keyword cloud information.
  8 in total

1.  48,XYYY: a new syndrome?

Authors:  G S Schoepflin; W R Centerwall
Journal:  J Med Genet       Date:  1972-09       Impact factor: 6.318

2.  A 48,XYYY male: a somatic and psychiatric description.

Authors:  H Hunter; R Quaife
Journal:  J Med Genet       Date:  1973-03       Impact factor: 6.318

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

Authors:  P Barlow
Journal:  Humangenetik       Date:  1973

4.  A patient with 45XO-48XYYY mosaicism.

Authors:  D Cox; C L Berry
Journal:  J Med Genet       Date:  1967-06       Impact factor: 6.318

5.  [The XYY status in children].

Authors:  J Keutel; I Dauner
Journal:  Z Kinderheilkd       Date:  1969

6.  The developmental spectrum of proximal radioulnar synostosis.

Authors:  Alison M Elliott; Lisa Kibria; Martin H Reed
Journal:  Skeletal Radiol       Date:  2010-01       Impact factor: 2.199

7.  48,XYYY: A Rare Case Report.

Authors:  A S Sabnis; D Bhusare
Journal:  Balkan J Med Genet       Date:  2022-06-05       Impact factor: 0.810

8.  Rare 48, XYYY syndrome: case report and review of the literature.

Authors:  Maryam Abedi; Arash Salmaninejad; Ebrahim Sakhinia
Journal:  Clin Case Rep       Date:  2017-12-07
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.