Yong Qu

Clinical and Functional Characterization of a Human ORNT1 Mutation (T32R) in the Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) Syndrome

Jose A. Camacho, Rebecca Mardach, Natalia Rioseco‐Camacho et al. · Pediatric Research · 2006 · 34 citations · Full text

Urology, Mendelian Disorder, Genetic Disorder +7

Tetrasomy 15q25?qter: Cytogenetic and molecular characterization of an analphoid supernumerary marker chromosome

Amy G. Rowe, Liane Abrams, Yong Qu et al. · American Journal of Medical Genetics · 2000 · 32 citations

Cytogenetics, Genetics, Pathology +18

X-linked mental retardation syndrome with characteristic ?coarse? facial appearance, brachydactyly, and short stature maps to proximal Xq

Nancy J. Carpenter, Yong Qu, Mary Curtis et al. · American Journal of Medical Genetics · 1999 · 19 citations

MOLECULAR PRENATAL DIAGNOSIS OF GLYCOGEN STORAGE DISEASE TYPE Ia

Yong Qu, José E. Abdenur, CHRISTINE M. ENG et al. · Prenatal Diagnosis · 1996 · 16 citations

Molecular Prenatal Diagnosis, Genetic Testing, Prenatal Genetic Testing +15

Regional localization of a nonspecific X-linked mental retardation gene (MRX59) to Xp21.2-p22.2

Nancy J. Carpenter, W. Ted Brown, Yong Qu et al. · American Journal of Medical Genetics · 1999 · 16 citations

Regional Localization, Straight Theta, Developmental Biology +13