A.M. Lamhonwah

Identification of an altered splice site in Ashkenazi Tay-Sachs disease

Enrico Arpaia, Anne Dumbrille-Ross, Thomas Maler et al. · Nature · 1988 · 142 citations

Genetics, Pathogenesis, Pathology +5

Isolation of cDNA clones coding for the beta subunit of human beta-hexosaminidase.

Brian F. O’Dowd, F Quan, H.F. Willard et al. · Proceedings of the National Academy of Sciences · 1985 · 116 citations · Full text

Genetics, Glycobiology, Molecular Biology +21

Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genes.

A.M. Lamhonwah, Teresa J. Barankiewicz, H.F. Willard et al. · Proceedings of the National Academy of Sciences · 1986 · 102 citations · Full text

Genetics, Human Polymorphism, Dna Polymorphisms +18

Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus

Rikki Kolluri, Amro Shehabeldin, Monica Peacocke et al. · Human Molecular Genetics · 1995 · 100 citations

Mutations participating in interallelic complementation in propionic acidemia.

R A Gravel, Beverly R. Akerman, A.M. Lamhonwah et al. · PubMed · 1994 · 42 citations