22三体综合征的家族性发生情况。 - Suppr

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Familial occurrence of trisomy 22.

作者信息

Uchida I A, Ray M, McRae K N, Besant D F

出版信息

Am J Hum Genet. 1968 Mar;20(2):107-18.

PMID:5643178

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1706268/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d43/1706268/5cb8eb80b2dd/ajhg00386-0021-a.jpg

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[Apropos of a case of 22-trisomy].

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CHROMOSOMES IN COLOBOMA AND ANAL ATRESIA.

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A PROBABLE CASE OF INCOMPLETE TRISOMY OF A CHROMOSOME OF THE 13-15 GROUP.

J Med Genet. 1965 Jun;2(2):136-41. doi: 10.1136/jmg.2.2.136.

IDENTIFICATION OF THE MONGOLISM CHROMOSOME BY DNA REPLICATION ANALYSIS.

Am J Hum Genet. 1965 May;17(3):191-201.

DNA REPLICATION PATTERNS OF HUMAN CHROMOSOMES.

Cytogenetics. 1963;2:175-93. doi: 10.1159/000129778.

ENLARGED SHORT ARM OR SATELLITE REGION-A HERITABLE TRAIT PROBABLY UNASSOCIATED WITH DEVELOPMENTAL DISORDER.

Cytogenetics. 1963;2:129-39. doi: 10.1159/000129774.

MANDIBULOFACIAL DYSOSTOSIS. REPORT OF TWO CASES WITH CHROMOSOME ANALYSIS.

Am J Dis Child. 1964 Mar;107:304-7.

A familial chromosome abnormality associated with repeated abortions.

Cytogenetics. 1962;1:199-209. doi: 10.1159/000129729.

Another child with 47 chromosomes.

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An apparently identical extra autosome in two severely retarded sisters with multiple malformations.

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