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The emerging role of genomics in the diagnosis and workup of congenital urinary tract defects: a novel deletion syndrome on chromosome 3q13.31-22.1

✍ Scribed by Materna-Kiryluk, Anna; Kiryluk, Krzysztof; Burgess, Katelyn E.; Bieleninik, Arkadiusz; Sanna-Cherchi, Simone; Gharavi, Ali G.; Latos-Bielenska, Anna


Book ID
121582168
Publisher
Springer
Year
2013
Tongue
English
Weight
551 KB
Volume
29
Category
Article
ISSN
0931-041X

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