Literature DB >> 5146418

Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+).

H E Wyandt, F Hecht, E W Lovrien, R E Stewart.   

Abstract

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Year:  1971        PMID： 5146418     DOI： 10.1159/000130162

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


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  6 in total

1.  Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.

Authors:  R H Lindenbaum; M Bobrow
Journal:  J Med Genet       Date:  1975-03       Impact factor: 6.318

2.  A male infant with monosomy 21.

Authors:  Y Kaneko; T Ikeuchi; M Sasaki; Y Stakae; S Kuwajima
Journal:  Humangenetik       Date:  1975-08-29

3.  Monosomy 21: a new case confirmed by in situ hybridization.

Authors:  M C Pellissier; N Philip; M A Voelckel-Baeteman; M G Mattei; J F Mattei
Journal:  Hum Genet       Date:  1987-01       Impact factor: 4.132

4.  21 monosomy in a retarded female infant.

Authors:  K H Halloran; W R Breg; M J Mahoney
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

5.  Annotation: genetic effects of aneuploidy.

Authors:  L Sandler; F Hecht
Journal:  Am J Hum Genet       Date:  1973-05       Impact factor: 11.025

6.  Molecular and cytogenetic characterization of a de novo t(5p;21q) in a patient previously diagnosed as monosomy 21.

Authors:  M C Phelan; C C Morton; R E Stevenson; R E Tanzi; G D Stewart; P C Watkins; J F Gusella; J A Amos
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025
  6 in total

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