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Journal of Medical Genetics|October 1, 1989
Central nervous system malformations in Mohr's syndromeW Reardon, M G Harbord, M A Hall-Craggs, et al.Acta Neurologica Scandinavica|July 1, 1997
Linkage analysis between idiopathic generalized epilepsies and the GABA(A) receptor alpha5, beta3 and gamma3 subunit gene cluster on chromosome 15T Sander, R Kretz, M P Williamson, et al.American Journal of Medical Genetics|November 1, 1992
Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafnessW Reardon, S Roberts, P D Phelps, et al.Clinical Genetics|May 1, 1992
Lethal congenital erythroderma: a newly recognised genetic disorderJ P Shield, M R Judge, W Reardon, et al.Psychoneuroendocrinology|March 14, 2015
Estradiol and cortisol interactions in youth externalizing psychopathologyJennifer L Tackett, Kathleen W Reardon, Kathrin Herzhoff, et al.Journal of Medical Genetics|August 28, 1999
Prevalence, age of onset, and natural history of thyroid disease in Pendred syndromeW Reardon, R Coffey, T Chowdhury, et al.Clinical Dysmorphology|August 24, 2000
An unknown combination of infantile spasms, retinal lesions, facial dysmorphism and limb abnormalitiesA S Plomp, W Reardon, S Benton, et al.American Journal of Medical Genetics|August 1, 1994
Autosomal recessive congenital intrauterine infection-like syndrome of microcephaly, intracranial calcification, and CNS diseaseW Reardon, A Hockey, P Silberstein, et al.Clinical Genetics|August 18, 1999
Further evidence from two families that craniofrontonasal dysplasia maps to Xp22L J Pulleyn, R M Winter, W Reardon, et al.Journal of Medical Genetics|July 5, 2003
Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathyJ Kohlhase, L Schubert, M Liebers, et al.Pageof 16