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American Journal of Medical Genetics|June 28, 2001
Mother to son transmission of del(1) (q42.1q42.3)J A Sanford Hanna, S Ball, R A Pagon, et al.JAMA|March 11, 1983
Family studies in tuberous sclerosis. evaluation of apparently unaffected parentsS B Cassidy, R A Pagon, M Pepin, et al.The Journal of Pediatrics|April 1, 1983
Autosomal recessive eye and brain anomalies: Warburg syndromeR A Pagon, S K Clarren, D F Milam, et al.Clinical Dysmorphology|October 1, 1994
A contiguous gene deletion syndrome at 7q21-q22 and implications for a relationship between isolated ectrodactyly and syndromic ectrodactylyM E Nunes, R A Pagon, C J Disteche, et al.Journal of the American Medical Informatics Association : JAMIA|June 1, 2000
GeneClinics: a hybrid text/data electronic publishing model using XML applied to clinical genetic testingP Tarczy-Hornoch, P Shannon, P Baskin, et al.American Journal of Medical Genetics|November 1, 1991
Twin fetuses with abnormalities that overlap with three midline malformation complexesS R Hingorani, R A Pagon, T H Shepard, et al.Ophthalmic Paediatrics and Genetics|March 1, 1988
Heterozygote detection in X-linked recessive incomplete achromatopsiaR A Pagon, G E Chatrian, R D Hamer, et al.Annales De Genetique|September 1, 1978
Trisomy 3 (p23-pter) resulting from maternal translocation, t (3 ; 4)(p23 ; q35)A Schinzel, J W Hanson, R A Pagon, et al.The Journal of Pediatrics|September 1, 1988
Nonfluorescent dicentric Y in males with hypospadiasM Drummond-Borg, R A Pagon, C M Bradley, et al.AJR. American Journal of Roentgenology|November 1, 1987
Holoprosencephaly: prenatal sonographic diagnosisD A Nyberg, L A Mack, A Bronstein, et al.Pageof 9