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Lawrence C Layman

Showing results (51-60 of 104) with videos related to

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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.
The New England Journal of Medicine|July 12, 2013
Delayed puberty and estrogen resistance in a woman with estrogen receptor α variantSamuel D Quaynor, Earl W Stradtman, Hyung-Goo Kim, et al.
The Journal of Clinical Endocrinology and Metabolism|February 7, 2013
Liquid chromatography-tandem mass spectrometry analysis of human adrenal vein 19-carbon steroids before and after ACTH stimulationJuilee Rege, Yasuhiro Nakamura, Fumitoshi Satoh, et al.
American Journal of Obstetrics and Gynecology|April 23, 2005
Screening candidate genes for mutations in patients with hypogonadotropic hypogonadism using custom genome resequencing microarraysNing Xu, Robert H Podolsky, Pranav Chudgar, et al.
BMC Neurology|August 11, 2016
A microdeletion at Xq22.2 implicates a glycine receptor GLRA4 involved in intellectual disability, behavioral problems and craniofacial anomaliesJonathan D J Labonne, Tyler D Graves, Yiping Shen, et al.
Journal of Assisted Reproduction and Genetics|December 23, 2025
The prevalence of pathogenic variants in medically actionable genes among individuals with idiopathic hypogonadotropic hypogonadism/Kallmann syndromeJaclyn M Kwal, Lynn P Chorich, Anna Navitski, et al.
Molecular and Cellular Endocrinology|April 9, 2024
Prevalence of pathogenic variants and digenic disease in patients diagnosed with normosmic hypogonadotropic hypogonadism/Kallmann SyndromeAlexandra Poch, Michael P Dougherty, Robert A Roman, et al.
Scientific Reports|December 29, 2019
The Use of Whole Exome Sequencing in a Cohort of Transgender Individuals to Identify Rare Genetic VariantsJ Graham Theisen, Viji Sundaram, Mary S Filchak, et al.
Fertility and Sterility|October 27, 2007
Effects of follicle-stimulating hormone and human chorionic gonadotropin on gonadal steroidogenesis in two siblings with a follicle-stimulating hormone beta subunit mutationAdriana Lofrano-Porto, Luiz Augusto Casulari, Paula P Nascimento, et al.
Gene|August 23, 2015
Concomitant partial exon skipping by a unique missense mutation of RPS6KA3 causes Coffin-Lowry syndromeJonathan D J Labonne, Min Ji Chung, Julie R Jones, et al.
Pageof 11

Showing results (51-60 of 104) with videos related to

Sort By:
Pageof 11
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.
The New England Journal of Medicine|July 12, 2013
Delayed puberty and estrogen resistance in a woman with estrogen receptor α variantSamuel D Quaynor, Earl W Stradtman, Hyung-Goo Kim, et al.
The Journal of Clinical Endocrinology and Metabolism|February 7, 2013
Liquid chromatography-tandem mass spectrometry analysis of human adrenal vein 19-carbon steroids before and after ACTH stimulationJuilee Rege, Yasuhiro Nakamura, Fumitoshi Satoh, et al.
American Journal of Obstetrics and Gynecology|April 23, 2005
Screening candidate genes for mutations in patients with hypogonadotropic hypogonadism using custom genome resequencing microarraysNing Xu, Robert H Podolsky, Pranav Chudgar, et al.
BMC Neurology|August 11, 2016
A microdeletion at Xq22.2 implicates a glycine receptor GLRA4 involved in intellectual disability, behavioral problems and craniofacial anomaliesJonathan D J Labonne, Tyler D Graves, Yiping Shen, et al.
Journal of Assisted Reproduction and Genetics|December 23, 2025
The prevalence of pathogenic variants in medically actionable genes among individuals with idiopathic hypogonadotropic hypogonadism/Kallmann syndromeJaclyn M Kwal, Lynn P Chorich, Anna Navitski, et al.
Molecular and Cellular Endocrinology|April 9, 2024
Prevalence of pathogenic variants and digenic disease in patients diagnosed with normosmic hypogonadotropic hypogonadism/Kallmann SyndromeAlexandra Poch, Michael P Dougherty, Robert A Roman, et al.
Scientific Reports|December 29, 2019
The Use of Whole Exome Sequencing in a Cohort of Transgender Individuals to Identify Rare Genetic VariantsJ Graham Theisen, Viji Sundaram, Mary S Filchak, et al.
Fertility and Sterility|October 27, 2007
Effects of follicle-stimulating hormone and human chorionic gonadotropin on gonadal steroidogenesis in two siblings with a follicle-stimulating hormone beta subunit mutationAdriana Lofrano-Porto, Luiz Augusto Casulari, Paula P Nascimento, et al.
Gene|August 23, 2015
Concomitant partial exon skipping by a unique missense mutation of RPS6KA3 causes Coffin-Lowry syndromeJonathan D J Labonne, Min Ji Chung, Julie R Jones, et al.
Pageof 11