Literature DB >> 13701146

A child with 49 chromosomes.

M FRACCARO, K KAIJSER, J LINDSTEN.   

Abstract

Entities:  

Keywords:  CHROMOSOMES; GENITALIA, MALE/abnormalities

Mesh：

Year:  1960        PMID： 13701146     DOI： 10.1016/s0140-6736(60)91963-2

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


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  39 in total

Review 1.  SEX CHROMATIN.

Authors:  U MITTWOCH
Journal:  J Med Genet       Date:  1964-09       Impact factor: 6.318

Review 2.  [ON THE CLINICAL ASPECTS AND HISTOPATHOLOGY OF PRIMARY MALE HYPOGONADISM. 2. CASTRATISM AND SO-CALLED KLINEFELTER'S SYNDROME AS DISEASE FORMS WITH KNOWN ETIOLOGY].

Authors:  O HORNSTEIN
Journal:  Arch Klin Exp Dermatol       Date:  1963-09-02

3.  A BOY WITH XXXXY SEX CHROMOSOMES.

Authors:  M C JOSEPH; J M ANDERS; A I TAYLOR
Journal:  J Med Genet       Date:  1964-12       Impact factor: 6.318

4.  [Chromosome anomalies in the blood cells of a child with multiple abnormalities].

Authors:  R A PFEIFFER; G SCHELLONG; W KOSENOW
Journal:  Klin Wochenschr       Date:  1962-10-15

5.  Chromosome abnormality in mongolism.

Authors:  C E BLANK
Journal:  Proc R Soc Med       Date:  1962-06

6.  [On the significance and conclusiveness of nuclear sex diagnosis].

Authors:  C OVERZIER
Journal:  Klin Wochenschr       Date:  1961-06-01

7.  Sex chromosome aberrations in relation to neuropsychiatry.

Authors:  P E POLANI
Journal:  Proc R Soc Med       Date:  1961-08

8.  Brief report: a 48XXXY/49XXXXY male with expressive speech defect.

Authors:  R A Collacott; C Mitchell; L Dawes-Gamble; I D Young; D Duckett
Journal:  J Autism Dev Disord       Date:  1990-12

9.  47,XXY/48,XXXY/49,XXXXY mosaic with hydrocephaly: a case report and review of the literature.

Authors:  Jesús E Dueñas-Arias; Maribel Aguilar-Medina; Eliakym Arámbula-Meraz; Juliana B Valenzuela-Camacho; Angelina Vega-Solano; Julio Granados; Rosalío Ramos-Payán
Journal:  J Med Case Rep       Date:  2007-09-19

10.  Congenital knee dislocation in a 49,XXXXY boy.

Authors:  R H Sijmons; A J van Essen; J D Visser; M Iprenburg; G F Nelck; M L Vos-Bender; B de Jong
Journal:  J Med Genet       Date:  1995-04       Impact factor: 6.318
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