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Journal of Medical Genetics|June 1, 1997
Delineation of 14q32.3 deletion syndromeA P Ortigas, C K Stein, L L Thomson, et al.Clinical Genetics|February 1, 1986
Thymus deficiency in an infant with a chromosome t(18;22)(q12.2;p11.2)pat rearrangementP Bowen, H Pabst, D Berry, et al.American Journal of Medical Genetics|March 10, 2001
Syndrome of short stature, widow's peak, ptosis, posteriorly angulated ears, and joint problems: exclusion of the Aarskog (FGD1) gene as a candidate geneB J LaDine, J A Simmons, A E Shrimpton, et al.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1983
[Activity of the creatine kinase isoenzyme CK-BB in the serum of neonates as an indicator of perinatal damage to the central nervous system]N Heinbokel, J J Hoo, H W Goedde, et al.Human Reproduction (Oxford, England)|July 1, 1993
The effects on in-vitro fertilization of autoantibodies to spermatozoa in subfertile menS V Rajah, J M Parslow, R J Howell, et al.Clinical Genetics|September 1, 1979
Complex de novo rearrangement of chromosome 9 with clinical features of monosomy 9p syndromeJ J Hoo, M I Parslow, R L Shaw, et al.Clinical Genetics|March 1, 1990
Proximal 15q variant as possible pitfall in the cytogenetic diagnosis of Prader-Willi syndromeJ J Hoo, M C Chao, I P Samuel, et al.Sleep|March 5, 2004
Of sleep state and postnatal age on arousal responses induced by mild hypoxia in infantsPeter M Parslow, Richard Harding, T Michael Adamson, et al.Human Reproduction (Oxford, England)|March 1, 1994
Unilateral testicular obstruction: orchidectomy or reconstruction?W F Hendry, J M Parslow, M C Parkinson, et al.Clinical Genetics|April 1, 1985
Recurrent de novo interstitial deletion of 16q in two mentally retarded sistersJ J Hoo, R B Lowry, C C Lin, et al.Pageof 53