Literature DB >> 5501391

Familial normal-partial trisomy 16 with selective endoreduplication in malformed proband.

M E Drets, J H Cardoso, A H Delfino, J Carrau.   

Abstract

Mesh：

Year:  1970        PMID： 5501391     DOI： 10.1159/000130103

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


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  7 in total

1.  The cytogenetics of 90 patients with idiopathic mental retardation/malformation syndromes and of 90 normal subjects.

Authors:  C T Doyle
Journal:  Hum Genet       Date:  1976-07-27       Impact factor: 4.132

2.  Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics.

Authors:  G R Sutherland
Journal:  Am J Hum Genet       Date:  1979-03       Impact factor: 11.025

3.  [Inter- and intrachromosomal distribution of spontaneous achromatic lesions and chromatid breaks].

Authors:  G Obe
Journal:  Chromosoma       Date:  1971       Impact factor: 4.316

4.  Constitutional chromosomal breakage.

Authors:  F Giraud; S Ayme; J F Mattei; M G Mattei
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

5.  Additional manifestations of the Neu-Laxova syndrome.

Authors:  S B Turkel; A J Ebbin; J W Towner
Journal:  J Med Genet       Date:  1983-06       Impact factor: 6.318

6.  The problem of partial endoreduplication.

Authors:  C Stahl-Maugé; H D Hager; T M Schroeder
Journal:  Hum Genet       Date:  1978-11-24       Impact factor: 4.132

7.  Origin of symmetrical triradial chromosomes in human cells.

Authors:  E M Kuhn; E Therman
Journal:  Chromosoma       Date:  1982       Impact factor: 4.316
  7 in total

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