The use of cell markers in the study of human hematopoietic neoplasiaRASKIND, W. H; FIALKOW, P. J.Advances in cancer research. 1987, Vol 49, pp 127-167, issn 0065-230XArticle

T(8; 21) with a phenotype of chronic myeloid leukemiaRASKIND, W. H; PAPAYANNOPOULOU, T; HAMMOND, W. P et al.American journal of hematology. 1988, Vol 28, Num 4, pp 266-269, issn 0361-8609Article

Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosomes 8 and 11RASKIND, W. H; CONRAD, E. U; CHANSKY, H et al.American journal of human genetics. 1995, Vol 56, Num 5, pp 1132-1139, issn 0002-9297Article

Use of α interferon for the treatment of relapse of chronic myelogenous leukemia in chronic phase after allogeneic bone marrow transplantationHIGANO, C. S; RASKIND, W. H; SINGER, J. W et al.Blood. 1992, Vol 80, Num 6, pp 1437-1442, issn 0006-4971Article

Mutations in the EXT1 and EXT2 genes in hereditary multiple exostosesWUYTS, W; VAN HUL, W; MORTIER, G et al.American journal of human genetics. 1998, Vol 62, Num 2, pp 346-354, issn 0002-9297Article

Cellular biology of acute myelogenous leukemiaSMITH, F. O; RASKIND, W. H; FIALKOW, P. J et al.Journal of pediatric hematology/oncology. 1995, Vol 17, Num 2, pp 113-122, issn 1077-4114Article

Frequent loss of heterozygosity at the retinoblastoma locus in human esophageal cancersBOYNTON, R. F; HUANG, Y; MELTZER, S. J et al.Cancer research (Baltimore). 1991, Vol 51, Num 20, pp 5766-5769, issn 0008-5472Article

The natural history of hereditary multiple exostosesSCHMALE, G. A; CONRAD, E. U; RASKIND, W. H et al.Journal of bone and joint surgery. American volume. 1994, Vol 76, Num 7, pp 986-992, issn 0021-9355Article

Evidence for a polyclonal etiology of palmar fibromatosisCHANSKY, H. A; TRUMBLE, T. E; CONRAD, E. U et al.The Journal of hand surgery (St. Louis, Mo.). 1999, Vol 24A, Num 2, pp 339-344, issn 0363-5023Article

Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A)ALLIKMETS, R; RASKIND, W. H; HUTCHINSON, A et al.Human molecular genetics (Print). 1999, Vol 8, Num 5, pp 743-749, issn 0964-6906Article

Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q34RASKIND, W. H; BOLIN, T; WOLFF, J et al.Human genetics. 1998, Vol 102, Num 1, pp 93-97, issn 0340-6717Article

Further evidence for the existence of a clonal Ph-negative stage in some cases of Ph-positive chronic myelocytic leukemiaRASKIND, W. H; FERRARIS, A. M; VASNA NAJFELD et al.Leukemia. 1993, Vol 7, Num 8, pp 1163-1167, issn 0887-6924Article

Use of interferon alfa-2a to treat hematologic relapse for chronic myelogenous leukemia after bone marrow transplantationHIGANO, C. S; RASKIND, W. H; SINGER, J. W et al.Acta haematologica. 1993, Vol 89, pp 8-14, issn 0001-5792, SUP1Conference Paper

Identification of a highly polymorphic marker within intron 7 of the ALAS2 gene and suggestion of at least two loci for X-linked sideroblastic anemiaCOX, T. C; KOZMAN, H. M; RASKIND, W. H et al.Human molecular genetics (Print). 1992, Vol 1, Num 8, pp 639-641, issn 0964-6906Article

Mutations in the TSGA14 gene in Families With Autism Spectrum DisordersKORVATSKA, O; ESTES, A; MUNSON, J et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2011, Vol 156, Num 3, pp 303-311, issn 1552-4841, 9 p.Article

CAG repeat expansion in autosomal dominant familial spastic paraparesis : novel expansion in a subset of patientsBENSON, K. F; HORWITZ, M; WOLFF, J et al.Human molecular genetics (Print). 1998, Vol 7, Num 11, pp 1779-1786, issn 0964-6906Article

Inactivation of p53 and the development of tetraploidy in the elastase-SV40 T antigen transgenic mouse pancreasRAMEL, S; SANCHEZ, C. A; SCHIMKE, M. K et al.Pancreas. 1995, Vol 11, Num 3, pp 213-222, issn 0885-3177Article

Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome IIWUYTS, W; SARVAN RAMLAKHAN; CONRAD, E. U et al.American journal of human genetics. 1995, Vol 57, Num 2, pp 382-387, issn 0002-9297Article

Persistent clonal areas and clonal expansion in Barrett's esophagusRASKIND, W. H; NORWOOD, T; LEVINE, D. S et al.Cancer research (Baltimore). 1992, Vol 52, Num 10, pp 2946-2950, issn 0008-5472Article

17p allelic deletions and p53 protein overexpression in Barrett's adenocarcinomaBLOUNT, P. L; RAMEL, S; RASKIND, W. H et al.Cancer research (Baltimore). 1991, Vol 51, Num 20, pp 5482-5486, issn 0008-5472Article

Segregation analysis of phenotypic components of learning disabilities. I. Nonword memory and digit spanWIJSMAN, E. M; PETERSON, D; LEUTENEGGER, A.-L et al.American journal of human genetics. 2000, Vol 67, Num 3, pp 631-646, issn 0002-9297Article

Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiencyJØRGENSEN, A. L; PHILIP, J; RASKIND, W. H et al.American journal of human genetics. 1992, Vol 51, Num 2, pp 291-298, issn 0002-9297Article

Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher diseaseRASKIND, W. H; WILLIAMS, C. A; HUDSON, L. D et al.American journal of human genetics. 1991, Vol 49, Num 6, pp 1355-1360, issn 0002-9297Article

Host origin of marrow stromal cells obtained from marrow transplant recipients and transformed in vitro by Simian virus-40RASKIND, W. H; SINGER, J. W; MORGAN, C. A et al.Experimental hematology. 1988, Vol 16, Num 10, pp 827-830, issn 0301-472XArticle

Correlation between cytogenetic and molecular findings in human chronic myelogenous leukemia lines EM-2 and EM-3RASKIND, W. H; DISTECHE, C. M; KEATING, A et al.Cancer genetics and cytogenetics. 1987, Vol 25, Num 2, pp 271-284, issn 0165-4608Article