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American Journal of Medical Genetics|January 31, 1997
Bilateral sensorineural deafness and hydrocephalus due to foramen of Monro obstruction in sibs: a newly described autosomal recessive disorderA E Chudley, C McCullough, D W McCulloughBiochemical and Molecular Medicine|October 1, 1995
Frequency of FMR1 premutations in a consecutive newborn population by PCR screening of Guthrie blood spotsA J Dawson, B N Chodirker, A E ChudleyPediatric Cardiology|July 26, 2003
Pulmonary atresia with intact ventricular septum and major aortopulmonary collaterals: association with deletion 22q11.2C Li, A E Chudley, R Soni, et al.Clinical Genetics|November 15, 2005
Split hand foot malformation (SHFM)A M Elliott, J A Evans, A E ChudleyAmerican Journal of Medical Genetics|October 1, 1990
True precocious puberty in a girl with the fragile X syndromeP S Moore, A E Chudley, J S WinterAmerican Journal of Medical Genetics|May 30, 1998
Vertical transmission of the Ohdo blepharophimosis syndromeA A Mhanni, A J Dawson, A E ChudleyPediatric Radiology|January 1, 1991
Spondylometepiphyseal dysplasia congenita, Strudwick typeS M Shebib, A E Chudley, M H ReedAnnales De Genetique|January 1, 1985
A case of de novo trisomy 12p syndromeM Ray, A E Chudley, N Christie, et al.American Journal of Human Genetics|May 1, 1984
Fragile (X) X-linked mental retardation. II. Frequency and replication pattern of fragile (X)(q28) in heterozygotesJ H Knoll, A E Chudley, J W GerrardAmerican Journal of Medical Genetics|November 1, 1989
Familial duodenal atresia: a report of two families and reviewL G Best, N E Wiseman, A E ChudleyPageof 11