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Titre
PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans
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BSO - Titre
PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans
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DOI
DOI
10.1136/jmedgenet-2016-104435
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DOAI
DOAI
10.1136/jmedgenet-2016-104435
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Identifiant WoS
WOS:000403816600007
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Accès ouvert
OA - Non
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Source - Accès ouvert
OA - Non
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Type d'accès
Non OA
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Editeur
BMJ
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Source
JOURNAL OF MEDICAL GENETICS
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ISSN
0022-2593
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Type de document
Article
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Notoriété
4 - Excellente
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CNRS
Oui
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CNRS - Institut
INSB - Institut des sciences biologiques
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uid:/CRQ26T57
12/10/2021 14:52:45 (latest)
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