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R S Wilroy

Showing results (11-20 of 71) with videos related to

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Fertility and Sterility|January 1, 1984
Luteal phase inadequacy and a chromosomal anomaly in recurrent abortionA C Wentz, P Martens, R S Wilroy
Radiology|December 1, 1972
Neonatal hyperthyroidism with accelerated skeletal maturation, craniosynostosis, and brachydactylyW Riggs, R S Wilroy, J N Etteldorf
European Journal of Pediatrics|July 1, 1977
Tissue limited mosaicism for unbalanced autosomal translocation in a child with congenital anomalies and mental retardationR L Summitt, A T Tharapel, R S Wilroy
American Journal of Medical Genetics|December 11, 1996
Type 3 Pfeiffer syndrome with normal thumbsN C Kerr, R S Wilroy, R A Kaufman
Birth Defects Original Article Series|January 1, 1975
Partial trisomy for different segments of chromosome 13 in several individuals of the same familyR S Wilroy, R L Summitt, P R Martens
The Journal of Pediatrics|April 1, 1974
X-autosome translocation in normal mother and effectively 21-monosomic daughterR L Summitt, P R Martens, R S Wilroy
The Journal of Pediatrics|November 1, 1973
Accelerated skeletal maturation in infancy syndrome: report of a third caseR E Tipton, R S Wilroy, R L Summitt
American Journal of Medical Genetics|January 1, 1978
The Dubowitz syndromeR S Wilroy, R E Tipton, R L Summitt
Teratology|October 1, 1979
Prune perineumJ N Peeden, R S Wilroy, R G Soper
American Journal of Medical Genetics|January 20, 1997
Linkage analysis in a family with the Opitz GBBB syndrome refines the location of the gene in Xp22 to a 4 cM regionM May, S Huston, R S Wilroy, et al.
Pageof 8

Showing results (11-20 of 71) with videos related to

Sort By:
Pageof 8
Fertility and Sterility|January 1, 1984
Luteal phase inadequacy and a chromosomal anomaly in recurrent abortionA C Wentz, P Martens, R S Wilroy
Radiology|December 1, 1972
Neonatal hyperthyroidism with accelerated skeletal maturation, craniosynostosis, and brachydactylyW Riggs, R S Wilroy, J N Etteldorf
European Journal of Pediatrics|July 1, 1977
Tissue limited mosaicism for unbalanced autosomal translocation in a child with congenital anomalies and mental retardationR L Summitt, A T Tharapel, R S Wilroy
American Journal of Medical Genetics|December 11, 1996
Type 3 Pfeiffer syndrome with normal thumbsN C Kerr, R S Wilroy, R A Kaufman
Birth Defects Original Article Series|January 1, 1975
Partial trisomy for different segments of chromosome 13 in several individuals of the same familyR S Wilroy, R L Summitt, P R Martens
The Journal of Pediatrics|April 1, 1974
X-autosome translocation in normal mother and effectively 21-monosomic daughterR L Summitt, P R Martens, R S Wilroy
The Journal of Pediatrics|November 1, 1973
Accelerated skeletal maturation in infancy syndrome: report of a third caseR E Tipton, R S Wilroy, R L Summitt
American Journal of Medical Genetics|January 1, 1978
The Dubowitz syndromeR S Wilroy, R E Tipton, R L Summitt
Teratology|October 1, 1979
Prune perineumJ N Peeden, R S Wilroy, R G Soper
American Journal of Medical Genetics|January 20, 1997
Linkage analysis in a family with the Opitz GBBB syndrome refines the location of the gene in Xp22 to a 4 cM regionM May, S Huston, R S Wilroy, et al.
Pageof 8