A male infant with monosomy 21 View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1975-03

AUTHORS

Yasuhiko Kaneko, Tatsuro Ikeuchi, Motomichi Sasaki, Yoshio Satake, Shigeru Kuwajima

ABSTRACT

A male infant with total monosomy 21 identified by Q-, G- and R-banding is described. His main symptoms are hypertonia, micrognathia, microphthalmus, imperforate anus, ambiguous external genitalia, floating and malopposed thumbs, overlying fingers, right clubfoot and growth retardation. Both parents are phenotypically as well as karotypically normal.

PAGES

1-7

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00273344

DOI

http://dx.doi.org/10.1007/bf00273344

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1040331417

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/1176129


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