Literature DB >> 7471509

Monosomy 10qter due to a balanced familial translocation: t(10;16)(q25.2;q24).

R D Wegner, J Kunze, H Paust.   

Abstract

Mesh：

Year:  1981        PMID： 7471509     DOI： 10.1111/j.1399-0004.1981.tb00683.x

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


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  5 in total

1.  Monosomy 10q26-qter and trisomy 11q13-qter as a result of de novo unbalanced translocation.

Authors:  F Tinsa; Y Chebbi; M Meddeb; D Bousnina; K Boussetta; S Bousnina
Journal:  J Appl Genet       Date:  2009       Impact factor: 3.240

2.  Terminal deletion of the long arm of chromosome 10.

Authors:  H Curtis; R T Howell; C Cope
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

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.  A case of interstitial deletion of 10q25.2----q26.1.

Authors:  D E Rooney; K Williams; D V Coleman; A Habel
Journal:  J Med Genet       Date:  1989-01       Impact factor: 6.318

5.  Partial trisomy 3p in two siblings: clinical and pathological findings.

Authors:  N Van Regemorter; E Vamos; Y Gillerot; V Viteux; F Hayez; A Pardou; J Flament-Durand
Journal:  Eur J Pediatr       Date:  1983-10       Impact factor: 3.183
  5 in total

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