L1CAM mutation in association with X-linked hydrocephalus and Hirschsprung’s disease

Por Jackson, Sha-Ron, Guner, Yigit S., Woo, Russell, Randolph, Linda M., Ford, Henri, Shin, Cathy E.
Publicado em 2009

Galsulfase (Naglazyme®) therapy in infants with mucopolysaccharidosis VI

Por Harmatz, Paul R., Garcia, Paula, Guffon, Nathalie, Randolph, Linda M., Shediac, Renée, Braunlin, Elizabeth, Lachman, Ralph S., Decker, Celeste
Publicado em 2013

Microdeletion del(22)(q12.2) encompassing the facial development-associated gene, MN1 (meningioma 1) in a child with Pierre-Robin sequence (including cleft palate) and neurofibroma...

Por Davidson, Tom B, Sanchez-Lara, Pedro A, Randolph, Linda M, Krieger, Mark D, Wu, Shi-Qi, Panigrahy, Ashok, Shimada, Hiroyuki, Erdreich-Epstein, Anat
Publicado em 2012

Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utility

Por Wang, Jia-Chi, Ross, Leslie, Mahon, Loretta W, Owen, Renius, Hemmat, Morteza, Wang, Boris T, El Naggar, Mohammed, Kopita, Kimberly A, Randolph, Linda M, Chase, John M, Matas Aguilera, Maria J, Siles, Juan López, Church, Joseph A, Hauser, Natalie, Shen, Joseph J, Jones, Marilyn C, Wierenga, Klaas J, Jiang, Zhijie, Haddadin, Mary, Boyar, Fatih Z, Anguiano, Arturo, Strom, Charles M, Sahoo, Trilochan
Publicado no Eur J Hum Genet (2015)