Literature DB >> 14041555

[Chromosomal translocation in a mentally deficient child with cryptorchidism].

E M BUHLER, R ROSSIER, I BODIS, V VULLIET, U K BUHLER, G STALDER.   

Abstract

Entities:  

Keywords:  CHROMOSOMES; CRYPTORCHISM; MENTAL DEFICIENCY; OBESITY

Mesh：

Year:  1963        PMID： 14041555     DOI： 10.1111/j.1651-2227.1963.tb03762.x

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN： 0365-1436            Impact factor:   2.299


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  11 in total

1.  The Prader-Willi syndrome with a 15/15 translocation. Case report and review of the literature.

Authors:  C J Hawkey; A Smithies
Journal:  J Med Genet       Date:  1976-04       Impact factor: 6.318

2.  The Prader-Willi syndrome with a 15/3 translocation.

Authors:  M Kucerová; M Straková; Z Polívková
Journal:  J Med Genet       Date:  1979-06       Impact factor: 6.318

3.  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

4.  Translocations of D chromosomes in two families: t(13q14q) and t(13q14q)+(13p14p).

Authors:  C G Palmer; P M Conneally; J C Christian
Journal:  J Med Genet       Date:  1969-06       Impact factor: 6.318

5.  Inherited t(13q14q) in two retarded sisters.

Authors:  B F Crandall; U Francke; M A Campbell; R S Sparkes
Journal:  Am J Hum Genet       Date:  1972-07       Impact factor: 11.025

6.  Di Guglielmo syndrome in a t(DgDg) heterozygote.

Authors:  B Dallapiccola; P Malacarne
Journal:  J Med Genet       Date:  1971-06       Impact factor: 6.318

7.  Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome.

Authors:  M G Butler; F J Meaney; C G Palmer
Journal:  Am J Med Genet       Date:  1986-03

8.  15/15 translocation in Prader-Willi syndrome.

Authors:  M Fraccaro; O Zuffardi; E M Buhler; L P Jurik
Journal:  J Med Genet       Date:  1977-08       Impact factor: 6.318

9.  Transmission of a D/D reciprocal translocation in a family with high incidence of mental retardation.

Authors:  A S Dekaban
Journal:  Am J Hum Genet       Date:  1966-05       Impact factor: 11.025

10.  Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment.

Authors:  M Fraccaro; O Zuffardi; E Bühler; A Schinzel; G Simoni; R Witkowski; E Bonifaci; D Caufin; G Cignacco; N Delendi
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132
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