Literature DB >> 3829444

Inv(4)(p16q21). A five-generation pedigree with 24 carriers and no recombinants.

F Rivas, L García-Esquivel, H Rivera, M E Jiménez, R M González, J M Cantú.   

Abstract

A familial inv(4)(p16q21) ascertained through a woman who had a thanatophoric dwarf daughter and two abortions is presented. She and 23 other relatives were carriers, but no recombinants were found. The proportion of abortions and neonatal deaths in carriers' offspring was similar to that in non-carriers. A random segregation of the inverted chromosome was observed. The analysis of the present and previous familial chromosome 4 pericentric inversions indicates that: the breakpoint in q, with a limit between q21 and q25 determines the occurrence of inherited unbalances, and most recombinant chromosomes have duplication of the larger distal segment.

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Year:  1987        PMID: 3829444     DOI: 10.1111/j.1399-0004.1987.tb02776.x

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


  3 in total

1.  Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversion.

Authors:  V Shashi; W L Golden; P S Allinson; S H Blanton; C von Kap-Herr; T E Kelly
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

2.  Paternal pericentric inversion of chromosome 4 as a cause of recurrent pregnancy loss.

Authors:  G C Wolf; J Mao; L Izquierdo; G Joffe
Journal:  J Med Genet       Date:  1994-02       Impact factor: 6.318

3.  A contribution to the differential diagnosis of the "group of schizophrenias": structural abnormality of chromosome 4.

Authors:  R M Palmour; S Miller; A Fielding; M Vekemans; F R Ervin
Journal:  J Psychiatry Neurosci       Date:  1994-07       Impact factor: 6.186

  3 in total

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