✦ LIBER ✦
Prenatal findings in a fetus with contiguous gene syndrome caused by deletion of Xp22.3 that includes locus for X-linked recessive type of chondrodysplasia punctata (CDPX1)
✍ Scribed by Tsuguhiro Horikoshi; Akihiko Kikuchi; Shunsuke Tamaru; Kyoko Ono; Mariko Kita; Kimiyo Takagi; Susumu Miyashita; Hiroshi Kawame; Osamu Shimokawa; Naoki Harada
- Book ID
- 109007262
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 600 KB
- Volume
- 36
- Category
- Article
- ISSN
- 1341-8076
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