Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Lawrence C Layman

Showing results (31-40 of 104) with videos related to

Pageof 11
Sort By:
Seminars in Reproductive Medicine|March 11, 2026
Clinical Testing for Genetic ConditionsHyung-Goo Kim, Sumia Brakta, Afif Ben-Mahmoud, et al.
Fertility and Sterility|June 17, 2008
Phenotypic spectrum of 45,X/46,XY males with a ring Y chromosome and bilaterally descended testesLawrence C Layman, Sandra P T Tho, Andrew D Clark, et al.
Molecular Genetics and Genomics : MGG|October 19, 2014
Novel MED12 gene somatic mutations in women from the Southern United States with symptomatic uterine fibroidsSunil K Halder, Archana Laknaur, Jessica Miller, et al.
Molecular and Cellular Endocrinology|October 21, 2017
JAK/STAT signaling pathway gene expression is reduced following Nelf knockdown in GnRH neuronsEun Kyung Ko, Lynn P Chorich, Megan E Sullivan, et al.
F&S Science|June 28, 2024
Identification of rare genetic variants in the PCDH genetic family in a cohort of transgender womenJohn G Theisen, Lynn P Chorich, Hongyan Xu, 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.
Best Practice & Research. Clinical Obstetrics & Gynaecology|June 4, 2017
Genetic basis of eugonadal and hypogonadal female reproductive disordersTatiana Trofimova, Daria Lizneva, Larisa Suturina, et al.
The Journal of Clinical Endocrinology and Metabolism|January 4, 2007
A mutation in the fibroblast growth factor receptor 1 gene causes fully penetrant normosmic isolated hypogonadotropic hypogonadismNing Xu, Yu Qin, Richard H Reindollar, et al.
American Journal of Medical Genetics. Part A|September 4, 2015
A microdeletion encompassing PHF21A in an individual with global developmental delay and craniofacial anomaliesJonathan D J Labonne, Julie Vogt, Lisa Reali, et al.
Molecular and Cellular Endocrinology|June 1, 2021
Genetics of hypogonadotropic Hypogonadism-Human and mouse genes, inheritance, oligogenicity, and genetic counselingErica D Louden, Alexandra Poch, Hyung-Goo Kim, et al.
Pageof 11

Showing results (31-40 of 104) with videos related to

Sort By:
Pageof 11
Seminars in Reproductive Medicine|March 11, 2026
Clinical Testing for Genetic ConditionsHyung-Goo Kim, Sumia Brakta, Afif Ben-Mahmoud, et al.
Fertility and Sterility|June 17, 2008
Phenotypic spectrum of 45,X/46,XY males with a ring Y chromosome and bilaterally descended testesLawrence C Layman, Sandra P T Tho, Andrew D Clark, et al.
Molecular Genetics and Genomics : MGG|October 19, 2014
Novel MED12 gene somatic mutations in women from the Southern United States with symptomatic uterine fibroidsSunil K Halder, Archana Laknaur, Jessica Miller, et al.
Molecular and Cellular Endocrinology|October 21, 2017
JAK/STAT signaling pathway gene expression is reduced following Nelf knockdown in GnRH neuronsEun Kyung Ko, Lynn P Chorich, Megan E Sullivan, et al.
F&S Science|June 28, 2024
Identification of rare genetic variants in the PCDH genetic family in a cohort of transgender womenJohn G Theisen, Lynn P Chorich, Hongyan Xu, 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.
Best Practice & Research. Clinical Obstetrics & Gynaecology|June 4, 2017
Genetic basis of eugonadal and hypogonadal female reproductive disordersTatiana Trofimova, Daria Lizneva, Larisa Suturina, et al.
The Journal of Clinical Endocrinology and Metabolism|January 4, 2007
A mutation in the fibroblast growth factor receptor 1 gene causes fully penetrant normosmic isolated hypogonadotropic hypogonadismNing Xu, Yu Qin, Richard H Reindollar, et al.
American Journal of Medical Genetics. Part A|September 4, 2015
A microdeletion encompassing PHF21A in an individual with global developmental delay and craniofacial anomaliesJonathan D J Labonne, Julie Vogt, Lisa Reali, et al.
Molecular and Cellular Endocrinology|June 1, 2021
Genetics of hypogonadotropic Hypogonadism-Human and mouse genes, inheritance, oligogenicity, and genetic counselingErica D Louden, Alexandra Poch, Hyung-Goo Kim, et al.
Pageof 11