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Showing results (11-20 of 53) with videos related to

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American Journal of Human Genetics|October 1, 1990
Screening for cystic fibrosis carriersJ D Schulman, A Maddalena, S H Black, et al.
Obstetrics and Gynecology|October 1, 1995
DNA-based prenatal determination of the RhEe genotypeW C Spence, P Potter, A Maddalena, et al.
Prenatal Diagnosis|October 1, 1987
The association of congenital skin disorders with acetylcholinesterase in amniotic fluidD P Bick, E A Balkite, A Baumgarten, et al.
Journal of the Association of Genetic Technologists|May 17, 2017
Mosaic Trisomy 9p in a Patient with Mild Dysmorphic Features and Normal IntelligenceRandeep Brar, Donald G Basel, David P Bick, et al.
Journal of Autism and Developmental Disorders|September 1, 1987
Open trial effects of beta-blockers on speech and social behaviors in 8 autistic adultsJ J Ratey, J Bemporad, P Sorgi, et al.
Molecular Human Reproduction|May 9, 2008
The prevalence of intragenic deletions in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndromeJennifer R Pedersen-White, Lynn P Chorich, David P Bick, et al.
Fertility and Sterility|November 24, 1999
Mutation analysis of the EMX2 gene in Kallmann's syndromeH S Taylor, K Block, D P Bick, et al.
Fertility and Sterility|October 11, 2005
The prevalence of gonadotropin-releasing hormone receptor mutations in a large cohort of patients with hypogonadotropic hypogonadismBalasubramanian Bhagavath, Metin Ozata, I C Ozdemir, et al.
Molecular Human Reproduction|January 11, 2007
KAL1 mutations are not a common cause of idiopathic hypogonadotrophic hypogonadism in humansBalasubramanian Bhagavath, Ning Xu, Metin Ozata, et al.
Human Immunology|January 8, 2013
A simplified method for screening siblings for HLA identity using short tandem repeat (STR) polymorphismsJennifer J Schiller, Kathleen A Hopp, Bradley C Pietz, et al.
Pageof 6

Showing results (11-20 of 53) with videos related to

Sort By:
Pageof 6
American Journal of Human Genetics|October 1, 1990
Screening for cystic fibrosis carriersJ D Schulman, A Maddalena, S H Black, et al.
Obstetrics and Gynecology|October 1, 1995
DNA-based prenatal determination of the RhEe genotypeW C Spence, P Potter, A Maddalena, et al.
Prenatal Diagnosis|October 1, 1987
The association of congenital skin disorders with acetylcholinesterase in amniotic fluidD P Bick, E A Balkite, A Baumgarten, et al.
Journal of the Association of Genetic Technologists|May 17, 2017
Mosaic Trisomy 9p in a Patient with Mild Dysmorphic Features and Normal IntelligenceRandeep Brar, Donald G Basel, David P Bick, et al.
Journal of Autism and Developmental Disorders|September 1, 1987
Open trial effects of beta-blockers on speech and social behaviors in 8 autistic adultsJ J Ratey, J Bemporad, P Sorgi, et al.
Molecular Human Reproduction|May 9, 2008
The prevalence of intragenic deletions in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndromeJennifer R Pedersen-White, Lynn P Chorich, David P Bick, et al.
Fertility and Sterility|November 24, 1999
Mutation analysis of the EMX2 gene in Kallmann's syndromeH S Taylor, K Block, D P Bick, et al.
Fertility and Sterility|October 11, 2005
The prevalence of gonadotropin-releasing hormone receptor mutations in a large cohort of patients with hypogonadotropic hypogonadismBalasubramanian Bhagavath, Metin Ozata, I C Ozdemir, et al.
Molecular Human Reproduction|January 11, 2007
KAL1 mutations are not a common cause of idiopathic hypogonadotrophic hypogonadism in humansBalasubramanian Bhagavath, Ning Xu, Metin Ozata, et al.
Human Immunology|January 8, 2013
A simplified method for screening siblings for HLA identity using short tandem repeat (STR) polymorphismsJennifer J Schiller, Kathleen A Hopp, Bradley C Pietz, et al.
Pageof 6