Literature DB >> 5146417

Double monosomy mosaicism (45,X-45, XX,21-) in a retarded child with multiple congenital malformations.

F M Weber, R S Sparkes, H Muller.   

Abstract

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Year:  1971        PMID： 5146417     DOI： 10.1159/000130161

Source DB:  PubMed          Journal:  Cytogenetics        ISSN： 0011-4537


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  5 in total

1.  Trisomy 21 with 47,+18 lymphocyte cell line: double mitotic nondisjunction.

Authors:  M B Jenkins; R L Kriel; L Boyd; A Barnwell
Journal:  J Med Genet       Date:  1978-10       Impact factor: 6.318

2.  A low frequency mosaicism for monosomy 21 in a live born female.

Authors:  M Lee; D Rose; A Lazzarini; B R Rajendra; L J Sciorra
Journal:  Hum Genet       Date:  1979-10-02       Impact factor: 4.132

3.  Four new cases of ring 21 and 22 including familial transmission of ring 21.

Authors:  C G Palmer; M E Hodes; T Reed; J Kojetin
Journal:  J Med Genet       Date:  1977-02       Impact factor: 6.318

4.  The phenotype Ae1B: a probable result of chimerism.

Authors:  G H Longster; E A Robinson; D I North
Journal:  J Med Genet       Date:  1978-10       Impact factor: 6.318

Review 5.  Molecular genetics of human chromosome 21.

Authors:  P C Watkins; R E Tanzi; S V Cheng; J F Gusella
Journal:  J Med Genet       Date:  1987-05       Impact factor: 6.318
  5 in total

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