A.M. Lamhonwah - Concepedia

Author

A.M. Lamhonwah

Also Known As

A M Lamhonwah, A. M. Lamhonwah, A.-M Lamhonwah, A.-M. Lamhonwah, A.M. Lamhonwah, A.‐M. Lamhonwah, AM Lamhonwah

Publications

547

Citations

H-Index

Concepts

All Affiliations

A.M. Lamhonwah is an author at Hospital for Sick Children specializing in medicine, genetics, and molecular biology.

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	360
2	Molecular Biology	3	3	360
3	Natural Sciences	2	2	218
4	Biochemistry	2	2	218
5	Metabolism	1	1	102

A.M. Lamhonwah

Publications

518

Citations

H-Index

Page 1

	Year	Citations
Identification of an altered splice site in Ashkenazi Tay-Sachs disease Enrico Arpaia, Anne Dumbrille-Ross, Thomas Maler, Nature GeneticsPathogenesisPathologyMolecular BiologyAltered Splice Site	1988	142
Isolation of cDNA clones coding for the beta subunit of human beta-hexosaminidase. Brian F. O’Dowd, F Quan, H.F. Willard, Proceedings of the National Academy of Sciences GeneticsGlycobiologyMolecular BiologyMolecular GeneticsProtein Genetics	1985	116
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, Proceedings of the National Academy of Sciences GeneticsHuman PolymorphismDna PolymorphismsMolecular BiologyGene Characterization	1986	102
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, Human Molecular Genetics	1995	100
Mutations participating in interallelic complementation in propionic acidemia. R A Gravel, Beverly R. Akerman, A.M. Lamhonwah, PubMed	1994	42
Propionicacidemia: absence of alpha-chain mRNA in fibroblasts from patients of the pccA complementation group. A.M. Lamhonwah, R A Gravel PubMed	1987	16

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