Clinical Genetic Testing for Kallmann Syndrome

Por Layman, Lawrence C.
Publicado em 2013

The genetic basis of female reproductive disorders: Etiology and clinical testing

Por Layman, Lawrence C.
Publicado em 2013

Genetic Considerations in the Patient with Turner Syndrome—45,X with or without Mosaicism

Por Zhong, Quincy, Layman, Lawrence C.
Publicado em 2012

Role of ART in Imprinting Disorders

Por Eroglu, Ali, Layman, Lawrence C.
Publicado em 2012

The Role of CHD7 Mutations in Patients with Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome

Por Kim, Hyung-Goo, Layman, Lawrence C.
Publicado em 2011

The Molecular Basis of Impaired Follicle-Stimulating Hormone Action: Evidence From Human Mutations and Mouse Models

Por Siegel, Eric T., Kim, Hyung-Goo, Nishimoto, Hiromi Koso, Layman, Lawrence C.
Publicado em 2013

The Genotype and Phenotype of Patients with Gonadotropin Releasing Hormone Receptor Mutations

Por Kim, Hyung-Goo, Pedersen-White, Jennifer, Bhagavath, Balasubramanian, Layman, Lawrence C.
Publicado em 2010

Retrieval of rhesus monkey (Macaca mulatta) oocytes by ultrasound-guided needle aspiration: Problems and Solutions

Por Rodriguez, Nancy A., Si, Wei, Emmi, Adelina M., Layman, Lawrence C., Eroglu, Ali
Publicado em 2009

Interstitial microduplication at 2p11.2 in a patient with syndromic intellectual disability: 30-year follow-up

Por Jun, Kyung Ran, Ullmann, Reinhard, Khan, Saadullah, Layman, Lawrence C, Kim, Hyung-Goo
Publicado em 2014

Phenotypic spectrum of 45,X/46,XY males with a ring Y chromosome and bilaterally descended testes

Por Layman, Lawrence C., Tho, Sandra P.T., Clark, Andrew D., Kulharya, Anita, McDonough, Paul G.
Publicado em 2008

Novel MED12 gene somatic mutations in women from the Southern United States with symptomatic uterine fibroids

Por Halder, Sunil K., Laknaur, Archana, Miller, Jessica, Layman, Lawrence C., Diamond, Michael, Al-Hendy, Ayman
Publicado no Mol Genet Genomics (2014)

The prevalence of intragenic deletions in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome

Por Pedersen-White, Jennifer R., Chorich, Lynn P., Bick, David P., Sherins, Richard J., Layman, Lawrence C.
Publicado em 2008

The identification of HESX1 mutations in Kallmann syndrome

Por Newbern, Kayce, Natrajan, Nithya, Kim, Hyung-Goo, Chorich, Lynn .P., Halvorson, Lisa, Cameron, Richard S., Layman, Lawrence C.
Publicado em 2013

Spectrum of genes involved in a unique case of Potocki Schaffer syndrome with a large chromosome 11 deletion

Por Romeike, Bernd F.M., Shen, Yiping, Nishimoto, Hiromi Koso, Morton, Cynthia C., Layman, Lawrence C., Kim, Hyung-Goo
Publicado em 2014

Comparative deletion mapping at 1p31.3-p32.2 implies NFIA responsible for intellectual disability coupled with macrocephaly and the presence of several other genes for syndromic in...

Por Labonne, Jonathan D. J., Shen, Yiping, Kong, Il-Keun, Diamond, Michael P., Layman, Lawrence C., Kim, Hyung-Goo
Publicado no Mol Cytogenet (2016)

The Expression of the miR-25/93/106b Family of Micro-RNAs in the Adipose Tissue of Women With Polycystic Ovary Syndrome

Por Wu, Hsiao-Li, Heneidi, Saleh, Chuang, Tung-Yueh, Diamond, Michael P., Layman, Lawrence C., Azziz, Ricardo, Chen, Yen-Hao
Publicado no J Clin Endocrinol Metab (2014)

Delayed Puberty and Estrogen Resistance in a Woman with Estrogen Receptor α Variant

Por Quaynor, Samuel D., Stradtman, Earl W., Kim, Hyung-Goo, Shen, Yiping, Chorich, Lynn P., Schreihofer, Derek A., Layman, Lawrence C.
Publicado em 2013

Liquid Chromatography–Tandem Mass Spectrometry Analysis of Human Adrenal Vein 19-Carbon Steroids Before and After ACTH Stimulation

Por Rege, Juilee, Nakamura, Yasuhiro, Satoh, Fumitoshi, Morimoto, Ryo, Kennedy, Michael R., Layman, Lawrence C., Honma, Seijiro, Sasano, Hironobu, Rainey, William E.
Publicado em 2013

A microdeletion at Xq22.2 implicates a glycine receptor GLRA4 involved in intellectual disability, behavioral problems and craniofacial anomalies

Por Labonne, Jonathan D. J., Graves, Tyler D., Shen, Yiping, Jones, Julie R., Kong, Il-Keun, Layman, Lawrence C., Kim, Hyung-Goo
Publicado no BMC Neurol (2016)

The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome

Por Quaynor, Samuel D., Kim, Hyung-Goo, Cappello, Elizabeth M., Williams, Tiera, Chorich, Lynn P., Bick, David P., Sherins, Richard J., Layman, Lawrence C.
Publicado em 2011