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Paper Details

Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiency.
Hum Mutat
5
2022
Author NameAffiliation
Mahshid S AzamianBaylor College of Medicine
Mahshid S AzamianTexas Children's Hospital
Casie A GenettiBoston Children's Hospital, Harvard Medical School
Pankaj B AgrawalBoston Children's Hospital, Harvard Medical School
Pankaj B AgrawalThe Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School
Monica H WojcikThe Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School
Monica H WojcikBoston Children's Hospital and Harvard Medical School
Monica H WojcikBroad Center for Mendelian Genomics and Program in Medical and Population Genetics, Broad Institute of MIT and Harvard
Sally Ann LynchClinical Genetics
Stephen W SchererThe Hospital for Sick Children
Stephen W SchererUniversity of Toronto
Stephen W SchererThe Hospital for Sick Children
Stephen W SchererUniversity of Toronto
Anne O'Donnell-LuriaThe Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School
Anne O'Donnell-LuriaMassachusetts General Hospital
Anne O'Donnell-LuriaBroad Center for Mendelian Genomics and Program in Medical and Population Genetics, Broad Institute of MIT and Harvard
Anne O'Donnell-LuriaThe Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School
Anne O'Donnell-LuriaBroad Center for Mendelian Genomics and Program in Medical and Population Genetics, Broad Institute of MIT and Harvard
Anne O'Donnell-LuriaMassachusetts General Hospital
Seema R LalaniBaylor College of Medicine
Seema R LalaniTexas Children's Hospital
Evan E EichlerUniversity of Washington School of Medicine
Evan E EichlerHoward Hughes Medical Institute, University of Washington
Evan E EichlerUniversity of Washington School of Medicine
Evan E EichlerHoward Hughes Medical Institute, University of Washington
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