Similar frequency of paternal uniparental disomy involving chromosome 20q (patUPD20q) in Japanese and Caucasian patients affected by sporadic pseudohypoparathyroidism type Ib (sporPHP1B)

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Bone
Prif Awduron: Takatani, Rieko, Minagawa, Masanori, Molinaro, Angelo, Reyes, Monica, Kinoshita, Kaori, Takatani, Tomozumi, Kazukawa, Itsuro, Nagatsuma, Misako, Kashimada, Kenichi, Sato, Kenichi, Matsushita, Kazuyuki, Nomura, Fumio, Shimojo, Naoki, Jüppner, Harald
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2015
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4501871/
https://ncbi.nlm.nih.gov/pubmed/25997889
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2015.05.011
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