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The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
November 10, 2015
An Acute Encephalopathy Accelerated by a Large Amount of Milk Consumption
F Moien-Afshari, N Z Mirhosseini, E G Lemire, et al.
American Journal of Medical Genetics
|
February 25, 1998
SAMS: provisionally unique multiple congenital anomalies syndrome consisting of short stature, auditory canal atresia, mandibular hypoplasia, and skeletal abnormalities
E G Lemire, G E Hildes-Ripstein, M H Reed, et al.
Journal of Child Neurology
|
July 21, 2007
Peripheral neuropathy in a child with Cree leukodystrophy
R J Huntsman, S Seshia, N Lowry, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
February 16, 2011
Neuroimaging and neurophysiology studies in carriers of cree leukoencephalopathy
R J Huntsman, E G Lemire, C L Voll, et al.
Current Genetics
|
July 1, 1991
Alteration of the cytochrome c oxidase subunit 2 gene in the [exn-5] mutant of Neurospora crassa
E G Lemire, J A Percy, J M Correia, et al.
Current Genetics
|
October 1, 1994
Mutations in the structural gene for cytochrome c result in deficiency of both cytochromes aa3 and c in Neurospora crassa
D A Bottorff, S Parmaksizoglu, E G Lemire, et al.
American Journal of Medical Genetics. Part A
|
November 19, 2009
Father-to-son transmission of an X-linked gene: a case of paternal sex chromosome heterodisomy
R A Ferrier, R B Lowry, E G Lemire, et al.
American Journal of Medical Genetics
|
December 2, 1996
A familial disorder with duodenal atresia and tetralogy of Fallot
E G Lemire, J A Evans, N G Giddins, et al.
Journal of Pediatric Hematology/Oncology
|
October 27, 1998
Familial neuroblastoma: report of a kindred with later age at diagnosis
E G Lemire, B N Chodirker, G J Williams, et al.
Clinical Genetics
|
March 18, 2008
Family history as a predictor of uptake of cancer preventive procedures by women with a BRCA1 or BRCA2 mutation
K A Metcalfe, W D Foulkes, C Kim-Sing, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
November 10, 2015
An Acute Encephalopathy Accelerated by a Large Amount of Milk Consumption
F Moien-Afshari, N Z Mirhosseini, E G Lemire, et al.
American Journal of Medical Genetics
|
February 25, 1998
SAMS: provisionally unique multiple congenital anomalies syndrome consisting of short stature, auditory canal atresia, mandibular hypoplasia, and skeletal abnormalities
E G Lemire, G E Hildes-Ripstein, M H Reed, et al.
Journal of Child Neurology
|
July 21, 2007
Peripheral neuropathy in a child with Cree leukodystrophy
R J Huntsman, S Seshia, N Lowry, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
February 16, 2011
Neuroimaging and neurophysiology studies in carriers of cree leukoencephalopathy
R J Huntsman, E G Lemire, C L Voll, et al.
Current Genetics
|
July 1, 1991
Alteration of the cytochrome c oxidase subunit 2 gene in the [exn-5] mutant of Neurospora crassa
E G Lemire, J A Percy, J M Correia, et al.
Current Genetics
|
October 1, 1994
Mutations in the structural gene for cytochrome c result in deficiency of both cytochromes aa3 and c in Neurospora crassa
D A Bottorff, S Parmaksizoglu, E G Lemire, et al.
American Journal of Medical Genetics. Part A
|
November 19, 2009
Father-to-son transmission of an X-linked gene: a case of paternal sex chromosome heterodisomy
R A Ferrier, R B Lowry, E G Lemire, et al.
American Journal of Medical Genetics
|
December 2, 1996
A familial disorder with duodenal atresia and tetralogy of Fallot
E G Lemire, J A Evans, N G Giddins, et al.
Journal of Pediatric Hematology/Oncology
|
October 27, 1998
Familial neuroblastoma: report of a kindred with later age at diagnosis
E G Lemire, B N Chodirker, G J Williams, et al.
Clinical Genetics
|
March 18, 2008
Family history as a predictor of uptake of cancer preventive procedures by women with a BRCA1 or BRCA2 mutation
K A Metcalfe, W D Foulkes, C Kim-Sing, et al.
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of 2