Literature DB >> 3879153

A familial paracentric inv(1)(q42q44) resulting in a child with a del(1)(q42) karyotype.

M Speevak, A G Hunter, H Hughes, D M Cox.   

Abstract

The derivation of a 46,XY,del(1)(q42) chromosome complement in a mentally retarded child from a maternal paracentric inv(1)(q42q44) is discussed and the clinical findings are compared to previously reported cases of the same deletion syndrome.

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Year:  1985        PMID: 3879153

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


  1 in total

Review 1.  Paracentric inversions: a review.

Authors:  K Madan
Journal:  Hum Genet       Date:  1995-11       Impact factor: 4.132

  1 in total

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