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R S Wilroy

Showing results (41-50 of 71) with videos related to

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American Journal of Medical Genetics|January 1, 1992
Deletion of chromosome 15pter-->q11.2 due to t(Y;15) in a boy with Prader-Willi syndromeM B Qumsiyeh, J D Dalton, P L Gordon, et al.
American Journal of Medical Genetics|March 1, 1992
Identification of the origin of ring/marker chromosomes in patients with Ullrich-Turner syndrome using X and Y specific alpha satellite DNA probesS A Tharapel, R S Wilroy, A M Keath, et al.
The Journal of Pediatrics|January 1, 1974
Argininosuccinic aciduria: investigation of an affected familyG J Billmeier, S V Molinary, R S Wilroy, et al.
Birth Defects Original Article Series|January 1, 1976
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.
Birth Defects Original Article Series|January 1, 1979
Phenotypic heterogeneity in the Noonan syndromeR S Wilroy, R L Summitt, R E Tipton, et al.
Journal of Medical Genetics|August 1, 1990
Partial duplication of the long arm of chromosome 6: a clinically recognisable syndromeE K Pivnick, M B Qumsiyeh, A T Tharapel, et al.
Journal of Medical Genetics|May 1, 1993
Elucidation of the centromere involvement in an inversion (13) by fluorescent in situ hybridisationP L Gordon, J D Dalton, P R Martens, et al.
Birth Defects Original Article Series|January 1, 1978
X-autosome translocations: a reviewR L Summitt, R E Tipton, R S Wilroy, et al.
Annales De Genetique|January 1, 1983
Diploid-triploid mosaicism: delineation of the syndromeA T Tharapel, R S Wilroy, P R Martens, et al.
American Journal of Medical Genetics|January 1, 1979
Duplication 6q syndromeR E Tipton, J S Berns, W E Johnson, et al.
Pageof 8

Showing results (41-50 of 71) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics|January 1, 1992
Deletion of chromosome 15pter-->q11.2 due to t(Y;15) in a boy with Prader-Willi syndromeM B Qumsiyeh, J D Dalton, P L Gordon, et al.
American Journal of Medical Genetics|March 1, 1992
Identification of the origin of ring/marker chromosomes in patients with Ullrich-Turner syndrome using X and Y specific alpha satellite DNA probesS A Tharapel, R S Wilroy, A M Keath, et al.
The Journal of Pediatrics|January 1, 1974
Argininosuccinic aciduria: investigation of an affected familyG J Billmeier, S V Molinary, R S Wilroy, et al.
Birth Defects Original Article Series|January 1, 1976
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.
Birth Defects Original Article Series|January 1, 1979
Phenotypic heterogeneity in the Noonan syndromeR S Wilroy, R L Summitt, R E Tipton, et al.
Journal of Medical Genetics|August 1, 1990
Partial duplication of the long arm of chromosome 6: a clinically recognisable syndromeE K Pivnick, M B Qumsiyeh, A T Tharapel, et al.
Journal of Medical Genetics|May 1, 1993
Elucidation of the centromere involvement in an inversion (13) by fluorescent in situ hybridisationP L Gordon, J D Dalton, P R Martens, et al.
Birth Defects Original Article Series|January 1, 1978
X-autosome translocations: a reviewR L Summitt, R E Tipton, R S Wilroy, et al.
Annales De Genetique|January 1, 1983
Diploid-triploid mosaicism: delineation of the syndromeA T Tharapel, R S Wilroy, P R Martens, et al.
American Journal of Medical Genetics|January 1, 1979
Duplication 6q syndromeR E Tipton, J S Berns, W E Johnson, et al.
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