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Cytogenetics and Cell Genetics|January 1, 1996
The detection of contiguous gene deletions at the neurofibromatosis 1 locus with fluorescence in situ hybridizationK A Leppig, D Viskochil, S Neil, et al.
Pediatrics|February 11, 1997
Magnetic resonance imaging of brain anomalies in fetal alcohol syndromeV W Swayze, V P Johnson, J W Hanson, et al.
American Journal of Medical Genetics|March 1, 1996
Distinct 15q genotypes in Russell-Silver and ring 15 syndromesP K Rogan, J R Seip, D J Driscoll, et al.
Pediatric Nephrology (Berlin, Germany)|November 5, 1997
Renal structural-functional relationships in early diabetes mellitusE N Ellis, B A Warady, E G Wood, et al.
The Journal of Pediatrics|July 1, 1995
Correlation of severity and outcome with plasma sterol levels in variants of the Smith-Lemli-Opitz syndromeG S Tint, G Salen, A K Batta, et al.
American Journal of Medical Genetics|January 31, 1997
Treatment of Smith-Lemli-Opitz syndrome: results of a multicenter trialM Irons, E R Elias, D Abuelo, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 16, 1994
Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneityM Muenke, F Gurrieri, C Bay, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|June 19, 2004
Amifostine and autologous hematopoietic stem cell support of escalating-dose melphalan: a phase I studyG L Phillips, B Meisenberg, D E Reece, et al.
Bone Marrow Transplantation|February 10, 2004
Activity of single-agent melphalan 220-300 mg/m2 with amifostine cytoprotection and autologous hematopoietic stem cell support in non-Hodgkin and Hodgkin lymphomaG L Phillips, B R Meisenberg, D E Reece, et al.
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