Literature DB >> 4434650

A familial 10/13 translocation: partial trisomy C in an infant associated with familial 10/13 translocation.

M T Mulcahy, J Jenkyn, P L Masters.   

Abstract

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Year:  1974        PMID： 4434650     DOI： 10.1111/j.1399-0004.1974.tb02256.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  8 in total

1.  Familial C/D translocation t(9;13)(9p23.13q21) in a male associated with recurrent abortion.

Authors:  D Singh-Kahlon; A Serra
Journal:  Hum Genet       Date:  1976-08-30       Impact factor: 4.132

2.  The cytogenetics of 90 patients with idiopathic mental retardation/malformation syndromes and of 90 normal subjects.

Authors:  C T Doyle
Journal:  Hum Genet       Date:  1976-07-27       Impact factor: 4.132

3.  Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2).

Authors:  J Brusnický; K M van Heerden; G de Jong; A S Cronjé; A E Retief
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

4.  Partial trisomy 10q: a recognizable syndrome.

Authors:  J M Klep-de Pater; J B Bijlsma; H F de France; N J Leschot; M Duijndam-van den Berge; J O van Hemel
Journal:  Hum Genet       Date:  1979-01-19       Impact factor: 4.132

5.  Balanced translocation (10;13) in a father, ascertained through the study of meiosis in semen, and partial trisomy 10q in his son. Characterization of the region responsible for the partial trisomy 10q syndrome.

Authors:  R Miró; C Templado; M Ponsá; J Serradell; S Marina; J Egozcue
Journal:  Hum Genet       Date:  1980-02       Impact factor: 4.132

6.  Familial translocation t(10;21)(q22;q22).

Authors:  A Delicado; I L Pajares; P Vicente; F Hawkins
Journal:  Hum Genet       Date:  1979-09       Impact factor: 4.132

7.  Severe mental retardation in a boy with partial trisomy 10q and partial monosomy 2q.

Authors:  J A Sills; K E Buckton; J A Raeburn
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

8.  Distal trisomy 10q syndrome, report of a patient with duplicated q24.31 - qter, autism spectrum disorder and unusual features.

Authors:  Yasser Al-Sarraj; Hakam Abu Al-Khair; Rowaida Ziad Taha; Namat Khattab; Zakaria H El Sayed; Bushra Elhusein; Hatem El-Shanti
Journal:  Clin Case Rep       Date:  2014-07-25
  8 in total

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