Evaluation of Mayer-Rokitansky-Kuster-Hauser (MRKH) Patient Families by Whole Genome Sequencing

por Dougherty, Michael P, Chorich, Lynn P, Layman, Lawrence Clarke
Publicado 2021

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 2008

The Use of Whole Exome Sequencing in a Cohort of Transgender Individuals to Identify Rare Genetic Variants

por Theisen, J. Graham, Sundaram, Viji, Filchak, Mary S., Chorich, Lynn P., Sullivan, Megan E., Knight, James, Kim, Hyung-Goo, Layman, Lawrence C.
Publicado 2019

OR06-3 ESR1 Pathogenic Variant With Incomplete Estrogen Insensitivity

por Chorich, Lynn P, Diamond, Michael P, Hall, Janet E, Korach, Kenneth S, Layman, Lawrence C, Li, Yin, Liu, Haitao, Roman, Robert A
Publicado 2022

Long-term follow-up of females with unbalanced X;Y translocations—reproductive and nonreproductive consequences

por Dobek, Whitney A, Kim, Hyung-Goo, Walls, Cedric A, Chorich, Lynn P, Tho, Sandra PT, Wang, Zi-Xuan, McDonough, Paul G, Layman, Lawrence C
Publicado 2015

A balanced chromosomal translocation involving chromosomes 3 and 16 in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome reveals new candidate genes at 3p22.3 and 16p13.3

por Williams, Lacey S., Kim, Hyung-Goo, Kalscheuer, Vera M., Tuck, J. Matthew, Chorich, Lynn P., Sullivan, Megan E., Falkenstrom, Allison, Reindollar, Richard H., Layman, Lawrence C.
Publicado 2016

Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia

por Demir Eksi, Durkadin, Shen, Yiping, Erman, Munire, Chorich, Lynn P., Sullivan, Megan E., Bilekdemir, Meric, Yılmaz, Elanur, Luleci, Guven, Kim, Hyung-Goo, Alper, Ozgul M., Layman, Lawrence C.
Publicado 2018