Marion A. Maw

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

Osamu Ogawa, Michael R. Eccles, Jenny Szeto et al. · Nature · 1993 · 709 citations

Developmental Biology, Gene Expression, Medicine +3

Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

Françoise Denoyelle, Dominique Weil, Marion A. Maw et al. · Human Molecular Genetics · 1997 · 635 citations · Full text

Mutation of the gene encoding cellular retinaldehyde–binding protein in autosomal recessive retinitis pigmentosa

Marion A. Maw, Breandán N. Kennedy, Allison Knight et al. · Nature Genetics · 1997 · 329 citations

Ocular Disease, Retina, Photoreceptor Cell +5

A homozygous 1–base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese

Sigrid Fuchs, Mitsuru Nakazawa, Marion A. Maw et al. · Nature Genetics · 1995 · 301 citations

Biology, Oguchi Disease, Genetics +7

A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration

Marion A. Maw · Human Molecular Genetics · 2000 · 292 citations · Full text

Ocular Disease, Genetics, Retinal Therapies +16