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Abul Ahmed

Research Profile

Chemicals & Drugs

Disorders

Physiology

Germ-Line Mutation

Procedures

DNA Mutational Analysis

Geographic Areas

Anatomy

Chromosomes, Human, Pair 18

Activities & Behaviors

Molecular Epidemiology

Genes & Molecular Sequences

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Publications

TOP 3
James R Howe; Mohamed G Sayed; Abul F Ahmed; John C Ringold; J Larsen-Haidle; Anders Merg; Frank A Mitros; C A Vaccaro; GM Petersen; Francis M Giardiello; Susan Tinley; Lauri A Aaltonen; Henry T Lynch
The prevalence of MADH4 and BMPR1A mutations in juvenile polyposis and absence of BMPR2, BMPR1B, and ACVR1 mutations.
Mohamed G Sayed; Abul F Ahmed; J R Ringold; M E Anderson; Jennifer L Bair; Frank A Mitros; Henry T Lynch; Susan Tinley; GM Petersen; Francis M Giardiello; Bert Vogelstein; James R Howe
Germline SMAD4 or BMPR1A mutations and phenotype of juvenile polyposis.
James R Howe; Jason Shellnut; Brian Wagner; John C Ringold; Mohamed G Sayed; Abul F Ahmed; Patrick M Lynch; Christopher I Amos; Pertti Sistonen; Lauri A Aaltonen
Common deletion of SMAD4 in juvenile polyposis is a mutational hotspot.

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All Publications

2004: James R Howe; Mohamed G Sayed; Abul F Ahmed; John C Ringold; J Larsen-Haidle; Anders Merg; Frank A Mitros; C A Vaccaro; GM Petersen; Francis M Giardiello; Susan Tinley; Lauri A Aaltonen; Henry T Lynch
The prevalence of MADH4 and BMPR1A mutations in juvenile polyposis and absence of BMPR2, BMPR1B, and ACVR1 mutations.
Journal of medical genetics 2004;41(7):484-91.
2002: Mohamed G Sayed; Abul F Ahmed; J R Ringold; M E Anderson; Jennifer L Bair; Frank A Mitros; Henry T Lynch; Susan Tinley; GM Petersen; Francis M Giardiello; Bert Vogelstein; James R Howe
Germline SMAD4 or BMPR1A mutations and phenotype of juvenile polyposis.
Annals of surgical oncology 2002;9(9):901-6.
2002: James R Howe; Jason Shellnut; Brian Wagner; John C Ringold; Mohamed G Sayed; Abul F Ahmed; Patrick M Lynch; Christopher I Amos; Pertti Sistonen; Lauri A Aaltonen
Common deletion of SMAD4 in juvenile polyposis is a mutational hotspot.
American journal of human genetics 2002;70(5):1357-62.

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