A new case of proximal monosomy 1p36, extending the phenotype

Nuk Controls Pathfinding of Commissural Axons in the Mammalian Central Nervous System

Mark Henkemeyer, Donata Orioli, Jeffrey T. Henderson et al. · Cell · 1996 · 534 citations · Full text

Medicine, Neurobiology, Neuroscience +15

Further Delineation of Deletion 1p36 Syndrome in 60 Patients: A Recognizable Phenotype and Common Cause of Developmental Delay and Mental Retardation

Agatino Battaglia, H. Eugene Hoyme, Bruno Dallapiccola et al. · PEDIATRICS · 2008 · 310 citations

Life Sciences, Genetics, Pediatrics +17

Physical Map of 1p36, Placement of Breakpoints in Monosomy 1p36, and Clinical Characterization of the Syndrome

Heidi A. Heilstedt, Blake C. Ballif, L A Howard et al. · The American Journal of Human Genetics · 2003 · 296 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality

HA Heilstedt, B. C. Ballif, L. T. Howard et al. · Clinical Genetics · 2003 · 145 citations

Life Sciences, Genetics, Molecular Genetics +17

Identification of proximal 1p36 deletions using array‐CGH: a possible new syndrome

S‐HL Kang, A. Scheffer, Zhishuo Ou et al. · Clinical Genetics · 2007 · 57 citations

Life Sciences, Genetics, Molecular Genetics +17