[Masculin phenotype in a child with a predominant 46, XX clone].

Phénotype masculin chez un enfant présentant un clone majoritaire 46, XX

Pediatrie ·Vol. 30 ·No. 1 ·1975-00-00 ·Pages 73-6

Malka J, Dieterlen M, Hadjian AJ, Joannard A, Bost M, Jalbert P

Abstract

暂无摘要

MeSH Terms

Adolescent Chromosomes, Human, 21-22 and Y Clone Cells Humans Intellectual Disability/genetics Karyotyping Male Phenotype Sex Chromosome Aberrations/diagnosis

Authors & Affiliations

6 authors, click to expand affiliations / ORCID

Malka J

Dieterlen M

Hadjian A J

Joannard A

Bost M

Jalbert P

Article Info

Journal

Pediatrie

Abbr.

Pediatrie

ISSN

0031-4021

Published

1975-00-00

Pages

73-6

Language

fre

Region

France

NLM ID

0401127

Subset

External Links

PubMed source

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[Masculin phenotype in a child with a predominant 46, XX clone].

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