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Åland Island eye disease (Forsius-Eriksson ocular albinism) and an Xp21 deletion in a patient with duchenne muscular dystrophy, glycerol kinase deficiency, and congenital adrenal hypoplasia

✍ Scribed by Pillers, De-Ann M. ;Weleber, Richard G. ;Powell, Berkley R. ;Hanna, Cheryl E. ;Magenis, R. Ellen ;Buist, Neil R. M.


Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
582 KB
Volume
36
Category
Article
ISSN
0148-7299

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