Literature DB >> 14415502

[Chromosome aberrations and human diseases. XXY Klinefelter's syndrome from 46 chromosomes caused by T-T centromeric fusion].

J LEJEUNE, R TURPIN, J DECOURT.   

Abstract

Entities:  

Keywords:  CHROMOSOMES; KLINEFELTER'S SYNDROME/genetics

Mesh：

Year:  1960        PMID： 14415502

Source DB:  PubMed          Journal:  C R Hebd Seances Acad Sci        ISSN： 0001-4036


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  12 in total

1.  Klinefelter's syndrome associated with a D/D translocation.

Authors:  M Sparagana; G P Smith
Journal:  J Med Genet       Date:  1975-09       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.  Investigation of family showing transmission of a 13-15 chromosomal translocation (Denver classification).

Authors:  S WALKER; R HARRIS
Journal:  Br Med J       Date:  1962-07-07

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.  A probable XXYY sex determining mechanism in a mentally defective male with Klinefelter's syndrome.

Authors:  D H CARR; M L BARR; E R PLUNKETT
Journal:  Can Med Assoc J       Date:  1961-04-22       Impact factor: 8.262

6.  Delineation of Robertsonian translocations in man by means of chromosome banding.

Authors:  F S Hill; R L Summitt
Journal:  Eur J Pediatr       Date:  1977-11-04       Impact factor: 3.183

7.  Inheritance of an Abnormal Chromosome in Down's Syndrome (Mongolism) with Leukemia.

Authors:  J L German; A P Demayo; A G Bearn
Journal:  Am J Hum Genet       Date:  1962-03       Impact factor: 11.025

8.  Down's syndrome with a familial D/D reciprocal translocation and a G/G chromosome.

Authors:  H B Marsden; R I Mackay; A Murray; H E Ward
Journal:  J Med Genet       Date:  1966-03       Impact factor: 6.318

9.  A pericentric inversion of a chromosome 4 with a t(4q+10p-) and a familial t(DqDq) in a mentally retarded girl.

Authors:  S W Soukup; W Yarema; M Robinow
Journal:  Humangenetik       Date:  1974

10.  A case of double aneuploidy, 47,XXY,14-,t(13q14q)+, also probably homozygous for the cystic fibrosis gene.

Authors:  R H Lindenbaum; N L Blackwell; D J De Sa'
Journal:  J Med Genet       Date:  1972-06       Impact factor: 6.318
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