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R S Wilroy

Showing results (61-70 of 71) with videos related to

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Clinical Genetics|June 1, 1986
First trimester chorionic villi sampling and direct chromosome preparationsA T Tharapel, J V Dacus, S A Tharapel, et al.
American Journal of Human Genetics|March 1, 1993
Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductionsA T Tharapel, K P Anderson, J L Simpson, et al.
Fertility and Sterility|December 1, 1975
Polycystic ovarian disease, maturation arrest of spermiogenesis, and Klinefelter's syndrome in siblings of a family with familial hirsutismP N Cohen, J R Givens, W L Wiser, et al.
American Journal of Medical Genetics|May 8, 1995
Characterization of an unbalanced de novo rearrangement by microsatellite polymorphism typing and by fluorescent in situ hybridizationJ Zhao, P L Gordon, R S Wilroy, et al.
Cell|November 18, 1994
Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factorN G Pasteris, A Cadle, L J Logie, et al.
American Journal of Medical Genetics|March 21, 1998
Most Jacobsen syndrome deletion breakpoints occur distal to FRA11BR C Michaelis, G V Velagaleti, C Jones, et al.
Cytogenetics and Cell Genetics|August 18, 1999
Chromosome duplications and deletions and their mechanisms of originA T Tharapel, R C Michaelis, G V Velagaleti, et al.
American Journal of Medical Genetics|March 1, 1985
Genetic amniocentesis: a twelve years' experienceJ V Dacus, R S Wilroy, R L Summitt, et al.
American Journal of Perinatology|July 1, 1990
Diagnosis of trisomy 18 using spontaneously dividing cells from fetal umbilical cord blood: a novel approach for rapid late second and third trimester prenatal diagnosisA T Tharapel, M L Moretti, C M Meyers, et al.
Human Molecular Genetics|December 1, 1994
Linkage of Pfeiffer syndrome to chromosome 8 centromere and evidence for genetic heterogeneityN H Robin, G J Feldman, H F Mitchell, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
Clinical Genetics|June 1, 1986
First trimester chorionic villi sampling and direct chromosome preparationsA T Tharapel, J V Dacus, S A Tharapel, et al.
American Journal of Human Genetics|March 1, 1993
Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductionsA T Tharapel, K P Anderson, J L Simpson, et al.
Fertility and Sterility|December 1, 1975
Polycystic ovarian disease, maturation arrest of spermiogenesis, and Klinefelter's syndrome in siblings of a family with familial hirsutismP N Cohen, J R Givens, W L Wiser, et al.
American Journal of Medical Genetics|May 8, 1995
Characterization of an unbalanced de novo rearrangement by microsatellite polymorphism typing and by fluorescent in situ hybridizationJ Zhao, P L Gordon, R S Wilroy, et al.
Cell|November 18, 1994
Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factorN G Pasteris, A Cadle, L J Logie, et al.
American Journal of Medical Genetics|March 21, 1998
Most Jacobsen syndrome deletion breakpoints occur distal to FRA11BR C Michaelis, G V Velagaleti, C Jones, et al.
Cytogenetics and Cell Genetics|August 18, 1999
Chromosome duplications and deletions and their mechanisms of originA T Tharapel, R C Michaelis, G V Velagaleti, et al.
American Journal of Medical Genetics|March 1, 1985
Genetic amniocentesis: a twelve years' experienceJ V Dacus, R S Wilroy, R L Summitt, et al.
American Journal of Perinatology|July 1, 1990
Diagnosis of trisomy 18 using spontaneously dividing cells from fetal umbilical cord blood: a novel approach for rapid late second and third trimester prenatal diagnosisA T Tharapel, M L Moretti, C M Meyers, et al.
Human Molecular Genetics|December 1, 1994
Linkage of Pfeiffer syndrome to chromosome 8 centromere and evidence for genetic heterogeneityN H Robin, G J Feldman, H F Mitchell, et al.
Pageof 8