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Journal of Inherited Metabolic Disease|January 1, 1992
Carrier detection in glutaric aciduria type I using interleukin-2-dependent cultured lymphocytesL E Seargeant, A E Chudley, L A Dilling, et al.Prenatal Diagnosis|November 1, 1994
MSAFP levels and oesophageal atresiaB N Chodirker, A E Chudley, K M MacDonald, et al.American Journal of Medical Genetics|January 1, 1986
Autism in fragile X femalesR J Hagerman, A E Chudley, J H Knoll, et al.American Journal of Medical Genetics|September 1, 1988
Developmental delay, short stature, and minor facial anomalies in a child with ring chromosome 16B N Chodirker, M Ray, P J McAlpine, et al.American Journal of Medical Genetics|June 1, 1992
Transmission of the fra(X) haplotype from three nonpenetrant brothers to their affected grandsonsA J Kirkilionis, A E Chudley, C R Greenberg, et al.Human Genetics|January 1, 1984
Partial deficiency of hypoxanthine-guanine phosphoribosyltransferase with reduced affinity for PP-ribose-P in four related males with goutF F Snyder, A E Chudley, P M MacLeod, et al.American Journal of Medical Genetics|December 2, 1996
A familial disorder with duodenal atresia and tetralogy of FallotE G Lemire, J A Evans, N G Giddins, et al.American Journal of Medical Genetics|July 1, 1991
Newly recognized syndrome of cerebral, ocular, dental, auricular, skeletal anomalies: CODAS syndrome--a case reportS M Shebib, M H Reed, E P Shuckett, et al.American Journal of Medical Genetics|December 31, 1997
Low MSAFP levels and Williams syndromeB N Chodirker, C R Greenberg, N G Giddins, et al.Clinical Genetics|May 29, 2002
Identification of a dup(5)(p15.3) by multicolor bandingD Riordan, A Vust, D E Wickstrom, et al.Pageof 11