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Molecular Medicine Today
|
June 22, 2000
Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis
R J Leventer, D T Pilz, N Matsumoto, et al.
Neurology
|
September 30, 2005
A developmental and genetic classification for malformations of cortical development
A J Barkovich, R I Kuzniecky, G D Jackson, et al.
American Journal of Medical Genetics
|
September 24, 1999
X-linked lissencephaly with absent corpus callosum and ambiguous genitalia
W B Dobyns, E Berry-Kravis, N J Havernick, et al.
American Journal of Medical Genetics
|
December 14, 1999
Familial lissencephaly with cleft palate and severe cerebellar hypoplasia
B Kerner, J M Graham, J A Golden, et al.
Neurology
|
January 12, 2002
Classification system for malformations of cortical development: update 2001
A J Barkovich, R I Kuzniecky, G D Jackson, et al.
American Journal of Human Genetics
|
October 1, 1991
Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization
A Kuwano, S A Ledbetter, W B Dobyns, et al.
Neuropediatrics
|
November 9, 2000
Polymicrogyria and motor neuropathy in Micro syndrome
M C Nassogne, B Henrot, C Saint-Martin, et al.
Pediatric Neurology
|
February 1, 1994
Childhood stroke and lupus anticoagulant
J C Olson, R J Konkol, J C Gill, et al.
American Journal of Medical Genetics
|
September 1, 1985
Syndromes with lissencephaly. II: Walker-Warburg and cerebro-oculo-muscular syndromes and a new syndrome with type II lissencephaly
W B Dobyns, J B Kirkpatrick, H M Hittner, et al.
Journal of Child Neurology
|
October 8, 1999
Clinical nosologic and genetic aspects of Joubert and related syndromes
P F Chance, L Cavalier, D Satran, et al.
Page
of 16
Search research articles
Search
Showing results (51-60 of 151) with videos related to
Sort By:
Page
of 16
Molecular Medicine Today
|
June 22, 2000
Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis
R J Leventer, D T Pilz, N Matsumoto, et al.
Neurology
|
September 30, 2005
A developmental and genetic classification for malformations of cortical development
A J Barkovich, R I Kuzniecky, G D Jackson, et al.
American Journal of Medical Genetics
|
September 24, 1999
X-linked lissencephaly with absent corpus callosum and ambiguous genitalia
W B Dobyns, E Berry-Kravis, N J Havernick, et al.
American Journal of Medical Genetics
|
December 14, 1999
Familial lissencephaly with cleft palate and severe cerebellar hypoplasia
B Kerner, J M Graham, J A Golden, et al.
Neurology
|
January 12, 2002
Classification system for malformations of cortical development: update 2001
A J Barkovich, R I Kuzniecky, G D Jackson, et al.
American Journal of Human Genetics
|
October 1, 1991
Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization
A Kuwano, S A Ledbetter, W B Dobyns, et al.
Neuropediatrics
|
November 9, 2000
Polymicrogyria and motor neuropathy in Micro syndrome
M C Nassogne, B Henrot, C Saint-Martin, et al.
Pediatric Neurology
|
February 1, 1994
Childhood stroke and lupus anticoagulant
J C Olson, R J Konkol, J C Gill, et al.
American Journal of Medical Genetics
|
September 1, 1985
Syndromes with lissencephaly. II: Walker-Warburg and cerebro-oculo-muscular syndromes and a new syndrome with type II lissencephaly
W B Dobyns, J B Kirkpatrick, H M Hittner, et al.
Journal of Child Neurology
|
October 8, 1999
Clinical nosologic and genetic aspects of Joubert and related syndromes
P F Chance, L Cavalier, D Satran, et al.
Page
of 16