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Paper Details

Infant mortality: the contribution of genetic disorders.
J Perinatol
42
2019
Infant, chromosomal disorders, genetic disorder, genetic disorders, infant, infants, single, single gene disorders
Author NameAffiliation
Monica H WojcikBoston Children's Hospital, Harvard Medical School
Monica H WojcikBoston 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, Harvard Medical School
Monica H WojcikThe Broad Institute of MIT and Harvard
Heather L PatersonBoston Children's Hospital, Harvard Medical School
Heather L PatersonThe Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School
Casie A GenettiBoston Children's Hospital, Harvard Medical School
Casie A GenettiThe Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School
Jill A MaddenBoston Children's Hospital, Harvard Medical School
Jill A MaddenThe Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School
Timothy W YuBoston Children's Hospital, Harvard Medical School
Timothy W YuThe Broad Institute of MIT and Harvard
Timothy W YuThe Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School
Timothy W YuBoston Children's Hospital, Harvard Medical School
Timothy W YuThe Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School
Timothy W YuThe Broad Institute of MIT and Harvard
Pankaj B AgrawalBoston 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
Pankaj B AgrawalBoston Children's Hospital, Harvard Medical School
Pankaj B AgrawalThe Broad Institute of MIT and Harvard
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