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Exome sequencing in a family with an X-linked lethal malformation syndrome: clinical consequences of hemizygous truncating OFD1 mutations in male patients

✍ Scribed by Y Tsurusaki; T Kosho; K Hatasaki; Y Narumi; K Wakui; Y Fukushima; H Doi; H Saitsu; N Miyake; N Matsumoto


Book ID
119981561
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
871 KB
Volume
83
Category
Article
ISSN
0009-9163

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