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R S Wilroy

Showing results (21-30 of 71) with videos related to

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Pediatrics|March 1, 1979
Strychnine therapy in nonketotic hyperglycinemiaD Arneson, L T Ch'ien, P Chance, et al.
Birth Defects Original Article Series|January 1, 1977
Familial fatal neonatal radiculoneuropathyR C Gilmartin, W Gooch, R S Wilroy, et al.
Clinical Genetics|April 1, 1977
Apparently balanced de novo translocations in patients with abnormal phenotypes: report of 6 casesA T Tharapel, R L Summitt, R S Wilroy, et al.
Annales De Genetique|December 1, 1977
Partial monosomy and partial trisomy for different segments of chromosome 13 in several individuals of the same familyR S Wilroy, R L Summitt, P Martens, et al.
Prenatal Diagnosis|January 1, 1986
Pericentric inversion of chromosome 19: prenatal diagnosis and genetic counsellingA T Tharapel, J C Ward, L Wiggins, et al.
Archives of Otolaryngology (Chicago, Ill. : 1960)|August 1, 1983
Temporal bone findings in trisomy 13 with cyclopiaK Tomoda, J J Shea, R E Shenefelt, et al.
American Journal of Obstetrics and Gynecology|July 1, 1984
The concurrence of facioauriculovertebral spectrum and the Rokitansky syndromeH T Winer-Muram, D Muram, R S Wilroy, et al.
Cancer Genetics and Cytogenetics|March 15, 1986
Philadelphia chromosome-positive chronic myelocytic leukemia with a supplementary t(4;9)(q21;p22) and long survivalS A Tharapel, G I Plitman, A T Tharapel, et al.
The Journal of Pediatrics|February 1, 1983
Anterior sacral defects: an autosomal dominantly inherited conditionV D Yates, R S Wilroy, G L Whitington, et al.
American Journal of Medical Genetics|October 1, 1991
High resolution replication banding combined with in situ hybridization for the delineation of a subtle chromosome rearrangementM B Qumsiyeh, R S Wilroy, J N Peeden, et al.
Pageof 8

Showing results (21-30 of 71) with videos related to

Sort By:
Pageof 8
Pediatrics|March 1, 1979
Strychnine therapy in nonketotic hyperglycinemiaD Arneson, L T Ch'ien, P Chance, et al.
Birth Defects Original Article Series|January 1, 1977
Familial fatal neonatal radiculoneuropathyR C Gilmartin, W Gooch, R S Wilroy, et al.
Clinical Genetics|April 1, 1977
Apparently balanced de novo translocations in patients with abnormal phenotypes: report of 6 casesA T Tharapel, R L Summitt, R S Wilroy, et al.
Annales De Genetique|December 1, 1977
Partial monosomy and partial trisomy for different segments of chromosome 13 in several individuals of the same familyR S Wilroy, R L Summitt, P Martens, et al.
Prenatal Diagnosis|January 1, 1986
Pericentric inversion of chromosome 19: prenatal diagnosis and genetic counsellingA T Tharapel, J C Ward, L Wiggins, et al.
Archives of Otolaryngology (Chicago, Ill. : 1960)|August 1, 1983
Temporal bone findings in trisomy 13 with cyclopiaK Tomoda, J J Shea, R E Shenefelt, et al.
American Journal of Obstetrics and Gynecology|July 1, 1984
The concurrence of facioauriculovertebral spectrum and the Rokitansky syndromeH T Winer-Muram, D Muram, R S Wilroy, et al.
Cancer Genetics and Cytogenetics|March 15, 1986
Philadelphia chromosome-positive chronic myelocytic leukemia with a supplementary t(4;9)(q21;p22) and long survivalS A Tharapel, G I Plitman, A T Tharapel, et al.
The Journal of Pediatrics|February 1, 1983
Anterior sacral defects: an autosomal dominantly inherited conditionV D Yates, R S Wilroy, G L Whitington, et al.
American Journal of Medical Genetics|October 1, 1991
High resolution replication banding combined with in situ hybridization for the delineation of a subtle chromosome rearrangementM B Qumsiyeh, R S Wilroy, J N Peeden, et al.
Pageof 8