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European Journal of Human Genetics : EJHG|March 14, 2000
Refined mapping of the human serotonin transporter (SLC6A4) gene within 17q11 adjacent to the CPD and NF1 genesS Shen, S Battersby, M Weaver, et al.American Journal of Medical Genetics|December 31, 1997
Familial neurofibromatosis 1 microdeletions: cosegregation with distinct facial phenotype and early onset of cutaneous neurofibromataK A Leppig, P Kaplan, D Viskochil, et al.The Journal of Pediatrics|April 1, 1990
Pigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of ItoV P Sybert, R A Pagon, M Donlan, et al.The Journal of Investigative Dermatology|May 1, 1987
Keratinocytes cultured from subjects with ichthyosis vulgaris are phenotypically abnormalP Fleckman, K A Holbrook, B A Dale, et al.The Journal of Investigative Dermatology|April 1, 1983
Epidermolytic hyperkeratosis: ultrastructure and biochemistry of skin and amniotic fluid cells from two affected fetuses and a newborn infantK A Holbrook, B A Dale, V P Sybert, et al.Molecular Ecology|September 12, 1998
Sequence analysis of the mitochondrial DNA control region of ciscoes (genus Coregonus): taxonomic implications for the Great Lakes species flockK M Reed, M O Dorschner, T N Todd, et al.Pediatric Radiology|April 16, 1998
Osteogenesis imperfecta with joint contractures: bruck syndromeM F Blacksin, B A Pletcher, M DavidBlood|September 9, 2000
Evidence that juvenile myelomonocytic leukemia can arise from a pluripotential stem cellL J Cooper, K M Shannon, M R Loken, et al.The New England Journal of Medicine|September 8, 1983
Evaluation of a protocol for post-mortem examination of stillbirthsR F Mueller, V P Sybert, J Johnson, et al.Plastic and Reconstructive Surgery|November 1, 1991
Congenital bifid sternum: repair in early infancy and literature reviewB M Greenberg, J M Becker, B A PletcherPageof 189