G. Glóver

Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis

Karin Buiting, Bärbel Dittrich, Stephanie Groß et al. · The American Journal of Human Genetics · 1998 · 215 citations · Full text

Developmental Anomaly, Genetic Disorder, Genetics +8

FRAXE and mental retardation.

John C. Mulley, Shuancang Yu, Danuta Z. Loesch et al. · Journal of Medical Genetics · 1995 · 135 citations · Full text

Cytogenetics, Genetics, Genetic Epidemiology +18

Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twins.

H. Kruyer, Montserrat Milà, G. Glóver et al. · PubMed · 1994 · 96 citations

Screening for AZF Deletion in a Large Series of Severely Impaired Spermatogenesis Patients

MC Martínez, M. J. BERNABÉS, E. Gómez et al. · Journal of Andrology · 2000 · 72 citations · Full text

Spermatogenesis, Fertility, Cytogenetics +21

New strategy for the prenatal detection/exclusion of paternal cystic fibrosis mutations in maternal plasma

Ana Bustamante‐Aragonés, J. Gallego‐Merlo, María José Trujillo-Tiebas et al. · Journal of Cystic Fibrosis · 2008 · 59 citations · Full text

Genetic Testing, Mendelian Disorder, Prenatal Genetic Testing +14