Syed M. Jalal

Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients

Regina Ensenauer, Adewale Adeyinka, Heather C. Flynn et al. · The American Journal of Human Genetics · 2003 · 381 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Waldenstrom macroglobulinemia neoplastic cells lack immunoglobulin heavy chain locus translocations but have frequent 6q deletions

Roelandt F.J. Schop, W. Michael Kuehl, Scott A. Van Wier et al. · Blood · 2002 · 203 citations · Full text

Medicine, Genetics, Oncology +13

Highly Sensitive Fluorescence In Situ Hybridization Method to Detect Double BCR/ABL Fusion and Monitor Response to Therapy in Chronic Myeloid Leukemia

Gordon W. Dewald, William A. Wyatt, Amy L. Juneau et al. · Blood · 1998 · 190 citations · Full text

Medicine, Hematology, Oncology +14

Position Effects Due to Chromosome Breakpoints that Map ∼900 Kb Upstream and ∼1.3 Mb Downstream of SOX9 in Two Patients with Campomelic Dysplasia

Gopalrao V.N. Velagaleti, Gabriel A. Bien‐Willner, Jill K. Northup et al. · The American Journal of Human Genetics · 2005 · 181 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Rothmund-Thomson syndrome due toRECQ4 helicase mutations: Report and clinical and molecular comparisons with Bloom syndrome and Werner syndrome

Noralane M. Lindor, Yasuhiro Furuichi, Saori Kitao et al. · American Journal of Medical Genetics · 2000 · 177 citations

Life Sciences, Genetics, Molecular Genetics +17