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

by Jun, Kyung Ran, Ullmann, Reinhard, Khan, Saadullah, Layman, Lawrence C, Kim, Hyung-Goo
Published 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...

by Labonne, Jonathan D. J., Shen, Yiping, Kong, Il-Keun, Diamond, Michael P., Layman, Lawrence C., Kim, Hyung-Goo
Published 2016

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

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

Unique phenotype in a patient with CHARGE syndrome

by Jain, Shobhit, Kim, Hyung-Goo, Lacbawan, Felicitas, Meliciani, Irene, Wenzel, Wolfgang, Kurth, Ingo, Sharma, Josefina, Schoeneman, Morris, Ten, Svetlana, Layman, Lawrence C, Jacobson-Dickman, Elka
Published 2011

miRNA-93 Inhibits GLUT4 and Is Overexpressed in Adipose Tissue of Polycystic Ovary Syndrome Patients and Women With Insulin Resistance

by Chen, Yen-Hao, Heneidi, Saleh, Lee, Jung-Min, Layman, Lawrence C., Stepp, David W., Gamboa, Gloria Mabel, Chen, Bo-Shiun, Chazenbalk, Gregorio, Azziz, Ricardo
Published 2013

MicroRNA-223 Expression Is Upregulated in Insulin Resistant Human Adipose Tissue

by Chuang, Tung-Yueh, Wu, Hsiao-Li, Chen, Chen-Chun, Gamboa, Gloria Mabel, Layman, Lawrence C., Diamond, Michael P., Azziz, Ricardo, Chen, Yen-Hao
Published 2015

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

by Labonne, Jonathan D. J., Graves, Tyler D., Shen, Yiping, Jones, Julie R., Kong, Il-Keun, Layman, Lawrence C., Kim, Hyung-Goo
Published 2016

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

by 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.
Published 2016

Steric Clash in the SET Domain of Histone Methyltransferase NSD1 as a Cause of Sotos Syndrome and Its Genetic Heterogeneity in a Brazilian Cohort

by Ha, Kyungsoo, Anand, Priya, Lee, Jennifer A., Jones, Julie R., Kim, Chong Ae, Bertola, Debora Romeo, Labonne, Jonathan D. J., Layman, Lawrence C., Wenzel, Wolfgang, Kim, Hyung-Goo
Published 2016

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

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