Chromosomal Microarray Study in Prader-Willi Syndrome

por Butler, Merlin G., Hossain, Waheeda A., Cowen, Neil, Bhatnagar, Anish
Publicado 2023

Clinical genetics evaluation and testing of connective tissue disorders: a cross-sectional study

por Veatch, Olivia J., Steinle, Jacob, Hossain, Waheeda A., Butler, Merlin G.
Publicado 2022

Whole Exome Sequencing in Females with Autism Implicates Novel and Candidate Genes

por Butler, Merlin G., Rafi, Syed K., Hossain, Waheeda, Stephan, Dietrich A., Manzardo, Ann M.
Publicado 2015

Sex-Dimorphic Interactions of MAOA Genotype and Child Maltreatment Predispose College Students to Polysubstance Use

por Fite, Paula J., Brown, Shaquanna, Hossain, Waheeda A., Manzardo, Ann, Butler, Merlin G., Bortolato, Marco
Publicado 2020

Analysis of the Prader–Willi syndrome imprinting center using droplet digital PCR and next‐generation whole‐exome sequencing

por Hartin, Samantha N., Hossain, Waheeda A., Francis, David, Godler, David E., Barkataki, Sangjucta, Butler, Merlin G.
Publicado 2019

Genomic, Clinical, and Behavioral Characterization of 15q11.2 BP1-BP2 Deletion (Burnside-Butler) Syndrome in Five Families

por Baldwin, Isaac, Shafer, Robin L., Hossain, Waheeda A., Gunewardena, Sumedha, Veatch, Olivia J., Mosconi, Matthew W., Butler, Merlin G.
Publicado 2021

Connective Tissue Disorders and Fragile X Molecular Status in Females: A Case Series and Review

por Butler, Merlin G., Hossain, Waheeda A., Steinle, Jacob, Gao, Harry, Cox, Eleina, Niu, Yuxin, Quach, May, Veatch, Olivia J.
Publicado 2022

A Streamlined Approach to Prader-Willi and Angelman Syndrome Molecular Diagnostics

por Strom, Samuel P., Hossain, Waheeda A., Grigorian, Melina, Li, Mickey, Fierro, Joseph, Scaringe, William, Yen, Hai-Yun, Teguh, Mirandy, Liu, Joanna, Gao, Harry, Butler, Merlin G.
Publicado 2021