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Journal of Medical Genetics|July 1, 1989
A possible human homologue for the mouse mutant disorganisationR M Winter, D DonnaiJournal of Medical Genetics|January 1, 1988
Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndromeM Baraitser, R M WinterJournal of Medical Genetics|May 1, 1993
Linkage analysis of infantile pyloric stenosis and markers from chromosome 9q11-q33: no evidence for a major gene in this candidate regionE Chung, R Coffey, K Parker, et al.British Journal of Haematology|July 1, 1980
Hb F synthesis in sickle cell anaemia: a comparison of Saudi Arab cases with those of African originW G Wood, M E Pembrey, G R Serjeant, et al.Archives of Disease in Childhood|April 1, 1991
Nesidioblastosis: evidence for autosomal recessive inheritanceD A Woolf, J V Leonard, R C Trembath, et al.Nature Genetics|February 14, 1998
Localisation of a gene implicated in a severe speech and language disorderS E Fisher, F Vargha-Khadem, K E Watkins, et al.Journal of Medical Genetics|December 1, 1987
Multiple pterygium syndrome: evolution of the phenotypeE M Thompson, D Donnai, M Baraitser, et al.Clinical Dysmorphology|January 1, 1993
Unusual association of cerebral and renal abnormalitiesR M Winter, J S WigglesworthActa Ophthalmologica Scandinavica. Supplement|January 1, 1996
Midline craniofacial defects and morning glory disc anomaly. A distinct clinical entityR J Leitch, R M WinterHuman Genetics|January 1, 1982
Lethal, neonatal, short-limbed platyspondylic dwarfism. A further variant?R M Winter, E M ThompsonPageof 23