Similar frequency of paternal uniparental disomy involving chromosome 20q (patUPD20q) in Japanese and Caucasian patients affected by sporadic pseudohypoparathyroidism type Ib (sporPHP1B)-Reference-Cited by-同舟云学术

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

Published:2015-10 Issue: Volume:79 Page:15-20
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

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

Funder

National Institutes of Health

Ministry of Health, Labor and Welfare, Japan

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference44 articles.

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