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PMID: 4386467 Published · ppublish fre Journal Article

[Prader, Labhardt and Willi syndrome (study of 11 cases)].

Le syndrome de Prader, Labhardt et Willi (Etudy de onze observations)

Archives francaises de pediatrie ·Vol. 25 ·No. 2 ·1968-02-00 ·Pages 121-49

Gabilan JC, Royer P

Abstract

暂无摘要

MeSH Terms
Body Height Child Child, Preschool Chromosomes, Human, 13-15 Chromosomes, Human, 21-22 and Y Consanguinity Cryptorchidism/complications Diabetes Mellitus, Type 1/complications Factor IX Female Humans Hypoglycemia/complications Infant Infant, Newborn Intellectual Disability/complications Iodine Radioisotopes Male Mosaicism Neuromuscular Diseases/complications Obesity/complications Osteochondritis/complications Pregnancy Pregnancy Complications Scoliosis/complications Sex Chromosome Aberrations Strabismus/complications Thyroid Function Tests Trisomy
Chemicals
Iodine Radioisotopes Factor IX
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Gabilan J C
Royer P
Article Info
Journal
Archives francaises de pediatrie
Abbr.
Arch Fr Pediatr
ISSN
0003-9764
Published
1968-02-00
Pages
121-49
Language
fre
Region
France
NLM ID
0372421
Subset
IM
External Links
PubMed source
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