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Cancer Research|October 15, 1991
17p allelic deletions and p53 protein overexpression in Barrett's adenocarcinomaP L Blount, S Ramel, W H Raskind, et al.
Human Genetics|October 3, 2018
Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorderN H Chapman, R A Bernier, S J Webb, et al.
The New England Journal of Medicine|August 20, 1987
Clonal development, stem-cell differentiation, and clinical remissions in acute nonlymphocytic leukemiaP J Fialkow, J W Singer, W H Raskind, et al.
Molecular Psychiatry|March 9, 2005
A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiencyW H Raskind, R P Igo, N H Chapman, et al.
The Journal of Clinical Investigation|June 1, 1989
Clonal analysis of childhood acute lymphoblastic leukemia with "cytogenetically independent" cell populationsC H Pui, W H Raskind, G R Kitchingman, et al.
American Journal of Human Genetics|October 23, 1997
Genetic heterogeneity in familial acute myelogenous leukemia: evidence for a second locus at chromosome 16q21-23.2M Horwitz, K F Benson, F Q Li, et al.
Leukemia|July 1, 1993
Clonal remission in childhood acute myeloid leukemia is an infrequent eventF O Smith, W H Raskind, P Waldron, et al.
American Journal of Human Genetics|August 1, 1995
Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11W Wuyts, S Ramlakhan, W Van Hul, et al.
Cancer Research|October 15, 1991
Frequent loss of heterozygosity at the retinoblastoma locus in human esophageal cancersR F Boynton, Y Huang, P L Blount, et al.
Molecular Psychiatry|December 14, 2016
Association of rare missense variants in the second intracellular loop of Na<sub>V</sub>1.7 sodium channels with familial autismM Rubinstein, A Patowary, I B Stanaway, et al.
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