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David P Bick

Showing results (11-20 of 24) with videos related to

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The Journal of Molecular Diagnostics : JMD|November 20, 2018
Evaluation for Genetic Disorders in the Absence of a Clinical Indication for Testing: Elective Genomic TestingJames T Lu, Matthew Ferber, Jill Hagenkord, et al.
Fertility and Sterility|February 28, 2006
Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadismBalasubramanian Bhagavath, Robert H Podolsky, Metin Ozata, et al.
Fertility and Sterility|November 1, 2011
The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndromeSamuel D Quaynor, Hyung-Goo Kim, Elizabeth M Cappello, et al.
Journal of Pediatric Genetics|February 15, 2018
A Rare Combination of Functional Disomy Xp, Deletion Xq13.2-q28 Spanning the <i>XIST</i> Gene, and Duplication 3q25.33-q29 in a Female with der(X)t(X;3)(q13.2;q25.33)Jess F Peterson, Donald G Basel, David P Bick, et al.
American Journal of Medical Genetics. Part A|October 4, 2005
Interstitial deletion of chromosome 12q: genotype-phenotype correlation of two patients utilizing array comparative genomic hybridizationOphir D Klein, Philip D Cotter, Ann M Schmidt, et al.
Journal of Medical Genetics|November 14, 2006
Zoom-in comparative genomic hybridisation arrays for the characterisation of variable breakpoint contiguous gene syndromesJennifer J Johnston, Robert L Walker, Sean Davis, et al.
Molecular Genetics and Metabolism|September 20, 2015
Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United StatesMarcus J Miller, Lindsay C Burrage, James B Gibson, et al.
Physiological Genomics|February 10, 2012
Human gene copy number spectra analysis in congenital heart malformationsAoy Tomita-Mitchell, Donna K Mahnke, Craig A Struble, et al.
American Journal of Human Genetics|October 7, 2008
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndromeHyung-Goo Kim, Ingo Kurth, Fei Lan, et al.
Fertility and Sterility|February 9, 2011
Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndromeNing Xu, Hyung-Goo Kim, Balasubramanian Bhagavath, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
The Journal of Molecular Diagnostics : JMD|November 20, 2018
Evaluation for Genetic Disorders in the Absence of a Clinical Indication for Testing: Elective Genomic TestingJames T Lu, Matthew Ferber, Jill Hagenkord, et al.
Fertility and Sterility|February 28, 2006
Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadismBalasubramanian Bhagavath, Robert H Podolsky, Metin Ozata, et al.
Fertility and Sterility|November 1, 2011
The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndromeSamuel D Quaynor, Hyung-Goo Kim, Elizabeth M Cappello, et al.
Journal of Pediatric Genetics|February 15, 2018
A Rare Combination of Functional Disomy Xp, Deletion Xq13.2-q28 Spanning the <i>XIST</i> Gene, and Duplication 3q25.33-q29 in a Female with der(X)t(X;3)(q13.2;q25.33)Jess F Peterson, Donald G Basel, David P Bick, et al.
American Journal of Medical Genetics. Part A|October 4, 2005
Interstitial deletion of chromosome 12q: genotype-phenotype correlation of two patients utilizing array comparative genomic hybridizationOphir D Klein, Philip D Cotter, Ann M Schmidt, et al.
Journal of Medical Genetics|November 14, 2006
Zoom-in comparative genomic hybridisation arrays for the characterisation of variable breakpoint contiguous gene syndromesJennifer J Johnston, Robert L Walker, Sean Davis, et al.
Molecular Genetics and Metabolism|September 20, 2015
Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United StatesMarcus J Miller, Lindsay C Burrage, James B Gibson, et al.
Physiological Genomics|February 10, 2012
Human gene copy number spectra analysis in congenital heart malformationsAoy Tomita-Mitchell, Donna K Mahnke, Craig A Struble, et al.
American Journal of Human Genetics|October 7, 2008
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndromeHyung-Goo Kim, Ingo Kurth, Fei Lan, et al.
Fertility and Sterility|February 9, 2011
Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndromeNing Xu, Hyung-Goo Kim, Balasubramanian Bhagavath, et al.
Pageof 3