𝔖 Bobbio Scriptorium
✦   LIBER   ✦

OCRL1 mutation analysis in French Lowe syndrome patients: Implications for molecular diagnosis strategy and genetic counseling

✍ Scribed by Nicole Monnier; Véronique Satre; Eliane Lerouge; Florence Berthoin; Joël Lunardi


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
290 KB
Volume
16
Category
Article
ISSN
1059-7794

No coin nor oath required. For personal study only.