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W B Dobyns

Showing results (81-90 of 151) with videos related to

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Human Genetics|October 1, 1990
Rapid diagnosis of Miller-Dieker syndrome and isolated lissencephaly sequence by the polymerase chain reactionJ R Batanian, S A Ledbetter, R K Wolff, et al.
Nature|August 19, 1993
Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeatsO Reiner, R Carrozzo, Y Shen, et al.
American Journal of Medical Genetics|July 9, 1999
Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3T I Pollin, W B Dobyns, C A Crowe, et al.
American Journal of Human Genetics|November 1, 1988
Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndromeP vanTuinen, W B Dobyns, D C Rich, et al.
Neuropediatrics|August 26, 1998
Microlissencephaly: a heterogeneous malformation of cortical developmentA J Barkovich, D M Ferriero, R M Barr, et al.
Neuropediatrics|January 4, 2005
Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus: a rare brain malformation syndrome associated with mental retardation and seizuresG Mirzaa, N N Dodge, I Glass, et al.
Annals of Neurology|June 1, 1987
Familial cavernous malformations of the central nervous system and retinaW B Dobyns, V V Michels, R V Groover, et al.
Human Molecular Genetics|August 11, 1999
Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1D T Pilz, J Kuc, N Matsumoto, et al.
American Journal of Human Genetics|August 1, 2000
Somatic and germline mosaic mutations in the doublecortin gene are associated with variable phenotypesJ G Gleeson, S Minnerath, R I Kuzniecky, et al.
Advances in Neurology|September 29, 1998
Rapid-onset dystonia-parkinsonism: a report of clinical, biochemical, and genetic studies in two familiesA Brashear, I J Butler, L J Ozelius, et al.
Pageof 16

Showing results (81-90 of 151) with videos related to

Sort By:
Pageof 16
Human Genetics|October 1, 1990
Rapid diagnosis of Miller-Dieker syndrome and isolated lissencephaly sequence by the polymerase chain reactionJ R Batanian, S A Ledbetter, R K Wolff, et al.
Nature|August 19, 1993
Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeatsO Reiner, R Carrozzo, Y Shen, et al.
American Journal of Medical Genetics|July 9, 1999
Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3T I Pollin, W B Dobyns, C A Crowe, et al.
American Journal of Human Genetics|November 1, 1988
Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndromeP vanTuinen, W B Dobyns, D C Rich, et al.
Neuropediatrics|August 26, 1998
Microlissencephaly: a heterogeneous malformation of cortical developmentA J Barkovich, D M Ferriero, R M Barr, et al.
Neuropediatrics|January 4, 2005
Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus: a rare brain malformation syndrome associated with mental retardation and seizuresG Mirzaa, N N Dodge, I Glass, et al.
Annals of Neurology|June 1, 1987
Familial cavernous malformations of the central nervous system and retinaW B Dobyns, V V Michels, R V Groover, et al.
Human Molecular Genetics|August 11, 1999
Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1D T Pilz, J Kuc, N Matsumoto, et al.
American Journal of Human Genetics|August 1, 2000
Somatic and germline mosaic mutations in the doublecortin gene are associated with variable phenotypesJ G Gleeson, S Minnerath, R I Kuzniecky, et al.
Advances in Neurology|September 29, 1998
Rapid-onset dystonia-parkinsonism: a report of clinical, biochemical, and genetic studies in two familiesA Brashear, I J Butler, L J Ozelius, et al.
Pageof 16