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M M Barmada

Showing results (11-20 of 24) with videos related to

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Genomics|May 1, 1996
A gene for autosomal dominant congenital nystagmus localizes to 6p12J B Kerrison, V J Arnould, M M Barmada, et al.
Human Molecular Genetics|November 18, 1998
Hereditary lymphedema: evidence for linkage and genetic heterogeneityR E Ferrell, K L Levinson, J H Esman, et al.
Gastroenterology|September 13, 2000
SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitisR H Pfützer, M M Barmada, A P Brunskill, et al.
Translational Psychiatry|June 3, 2015
Genome-wide copy-number variation study of psychosis in Alzheimer's diseaseX Zheng, F Y Demirci, M M Barmada, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 16, 1999
Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3J B Kerrison, V J Arnould, J M Ferraz Sallum, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|May 25, 2005
The SPINK1 N34S mutation is not associated with Type 2 diabetes mellitus in a population of the USAA Schneider, E C Lawrence, M M Barmada, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2011
Replication study of genome-wide associated SNPs with late-onset Alzheimer's diseaseL C Burns, R L Minster, F Y Demirci, et al.
Journal of Medical Genetics|December 10, 2002
Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathyT C Hart, M C Gorry, P S Hart, et al.
American Journal of Human Genetics|June 23, 1998
Linkage and association between inflammatory bowel disease and a locus on chromosome 12R H Duerr, M M Barmada, L Zhang, et al.
Molecular Psychiatry|October 19, 2011
Genome-wide association analysis of age-at-onset in Alzheimer's diseaseM I Kamboh, M M Barmada, F Y Demirci, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Genomics|May 1, 1996
A gene for autosomal dominant congenital nystagmus localizes to 6p12J B Kerrison, V J Arnould, M M Barmada, et al.
Human Molecular Genetics|November 18, 1998
Hereditary lymphedema: evidence for linkage and genetic heterogeneityR E Ferrell, K L Levinson, J H Esman, et al.
Gastroenterology|September 13, 2000
SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitisR H Pfützer, M M Barmada, A P Brunskill, et al.
Translational Psychiatry|June 3, 2015
Genome-wide copy-number variation study of psychosis in Alzheimer's diseaseX Zheng, F Y Demirci, M M Barmada, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 16, 1999
Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3J B Kerrison, V J Arnould, J M Ferraz Sallum, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|May 25, 2005
The SPINK1 N34S mutation is not associated with Type 2 diabetes mellitus in a population of the USAA Schneider, E C Lawrence, M M Barmada, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2011
Replication study of genome-wide associated SNPs with late-onset Alzheimer's diseaseL C Burns, R L Minster, F Y Demirci, et al.
Journal of Medical Genetics|December 10, 2002
Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathyT C Hart, M C Gorry, P S Hart, et al.
American Journal of Human Genetics|June 23, 1998
Linkage and association between inflammatory bowel disease and a locus on chromosome 12R H Duerr, M M Barmada, L Zhang, et al.
Molecular Psychiatry|October 19, 2011
Genome-wide association analysis of age-at-onset in Alzheimer's diseaseM I Kamboh, M M Barmada, F Y Demirci, et al.
Pageof 3