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R S Wilroy

Showing results (51-60 of 71) with videos related to

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Southern Medical Journal|February 1, 1973
Neurologic manifestations of the Noonan syndromeD A Duenas, S Preissig, R L Summitt, et al.
American Journal of Medical Genetics|November 14, 2000
Localization of SRY by primed in situ labeling in XX and XY sex reversalJ S Kadandale, S S Wachtel, Y Tunca, et al.
American Journal of Medical Genetics|September 1, 1990
Adjacent-2 disjunction of a maternal t(9;22) leading to duplication 9pter----q22 and deficiency of 22pter----q11.2E K Pivnick, R S Wilroy, J B Summitt, et al.
Annales De Genetique|May 20, 2000
Hypomelanosis of ito and a 'mirror image' whole chromosome duplication resulting in trisomy 14 mosaicismY Tunca, R S Wilroy, J S Kadandale, et al.
Birth Defects Original Article Series|January 11, 1975
Hyperthecosis: an inheritable form of polycystic ovarian diseaseR S Wilroy, J R Givens, W L Wiser, et al.
Obstetrics and Gynecology|June 1, 1975
Features of Turner's syndrome in women with polycystic ovariesJ R Givens, R S Wilroy, R L Summitt, et al.
Prenatal Diagnosis|September 1, 1991
Prenatal counselling and diagnosis in progressively deforming osteogenesis imperfecta: a case of autosomal dominant transmissionO P Phillips, L P Shulman, L A Altieri, et al.
American Journal of Medical Genetics|December 1, 1983
Ring chromosome 6: variability in phenotypic expressionJ N Peeden, P Scarbrough, K Taysi, et al.
American Journal of Medical Genetics|July 11, 1991
Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probesA T Tharapel, M B Qumsiyeh, P R Martens, et al.
Journal of Medical Genetics|September 1, 1996
Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 casesE K Pivnick, G V Velagaleti, R S Wilroy, et al.
Pageof 8

Showing results (51-60 of 71) with videos related to

Sort By:
Pageof 8
Southern Medical Journal|February 1, 1973
Neurologic manifestations of the Noonan syndromeD A Duenas, S Preissig, R L Summitt, et al.
American Journal of Medical Genetics|November 14, 2000
Localization of SRY by primed in situ labeling in XX and XY sex reversalJ S Kadandale, S S Wachtel, Y Tunca, et al.
American Journal of Medical Genetics|September 1, 1990
Adjacent-2 disjunction of a maternal t(9;22) leading to duplication 9pter----q22 and deficiency of 22pter----q11.2E K Pivnick, R S Wilroy, J B Summitt, et al.
Annales De Genetique|May 20, 2000
Hypomelanosis of ito and a 'mirror image' whole chromosome duplication resulting in trisomy 14 mosaicismY Tunca, R S Wilroy, J S Kadandale, et al.
Birth Defects Original Article Series|January 11, 1975
Hyperthecosis: an inheritable form of polycystic ovarian diseaseR S Wilroy, J R Givens, W L Wiser, et al.
Obstetrics and Gynecology|June 1, 1975
Features of Turner's syndrome in women with polycystic ovariesJ R Givens, R S Wilroy, R L Summitt, et al.
Prenatal Diagnosis|September 1, 1991
Prenatal counselling and diagnosis in progressively deforming osteogenesis imperfecta: a case of autosomal dominant transmissionO P Phillips, L P Shulman, L A Altieri, et al.
American Journal of Medical Genetics|December 1, 1983
Ring chromosome 6: variability in phenotypic expressionJ N Peeden, P Scarbrough, K Taysi, et al.
American Journal of Medical Genetics|July 11, 1991
Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probesA T Tharapel, M B Qumsiyeh, P R Martens, et al.
Journal of Medical Genetics|September 1, 1996
Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 casesE K Pivnick, G V Velagaleti, R S Wilroy, et al.
Pageof 8