[FAMILIAL TURNER'S SYNDROME. STUDY OF 2 FAMILIES WITH XO AND XX KARYOTYPES].

LE SYNDROME DE TURNER FAMILIAL. ETUDE DE DEUX FAMILLES AVEC CARYOTYPES XO ET XX.

Annales de pediatrie ·Vol. 10 ·1963-04-02 ·Pages 163-7

JOSSO N, DE GROUCHY J, FREZAL J, LAMY M

Abstract

暂无摘要

Keywords

ADOLESCENCE CHROMOSOMES DIAGNOSIS GENETICS HUMAN TURNER'S SYNDROME

MeSH Terms

Adolescent Chromosomes Diagnosis Genetics, Medical Humans Karyotype Karyotyping Noonan Syndrome Turner Syndrome

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

JOSSO N

DE GROUCHY J

FREZAL J

LAMY M

Article Info

Journal

Annales de pediatrie

Abbr.

Ann Pediatr (Paris)

ISSN

0066-2097

Published

1963-04-02

Pages

163-7

Language

fre

Region

France

NLM ID

2984696R

Subset

External Links

PubMed source

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