Congenital Hypogonadotropic Hypogonadism and Cornelia de Lange Syndrome Share Clinical Phenotype and Genetic Background

AuthID
 P-00X-8Q1
13
Author(s)
Xu, C
·
Messina, A
·
Acierno, J
·
Niederlander, N
·
Santoni, F
·
Papadakis, G
·
Pignatelli, D
·
Stefanija, MA
·
Kimberly, KS
·
Balasubramanian, R
·
Crowley, W
·
Tipo de Documento
Abstract
Year published
2022
Publicado
in HORMONE RESEARCH IN PAEDIATRICS, ISSN: 1663-2818
Volume: 95, Número: SUPPL 2, Páginas: 352-352 (1)
Indexing
Wos®
Publication Identifiers
Wos: WOS:000854435701282
Source Identifiers
ISSN: 1663-2818
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