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Clinical Genetics
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April 19, 2011
Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformations
V Bhat, S C Girimaji, G Mohan, et al.
Clinical Genetics
|
June 24, 2011
Using Alzheimer's disease as a model for genetic risk disclosure: implications for personal genomics
J S Roberts, K D Christensen, R C Green
Clinical Genetics
|
June 24, 2011
Genotype-phenotype correlation in colorectal polyposis
K F Newton, E K L Mallinson, J Bowen, et al.
Clinical Genetics
|
December 16, 2010
Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome
L Raskin, F Schwenter, M Freytsis, et al.
Clinical Genetics
|
December 24, 2010
Congenital myasthenic syndrome associated with epidermolysis bullosa caused by homozygous mutations in PLEC1 and CHRNE
R A Maselli, J Arredondo, O Cagney, et al.
Clinical Genetics
|
January 5, 2011
Breast cancer after bilateral risk-reducing mastectomy
A-B Skytte, D Crüger, M Gerster, et al.
Clinical Genetics
|
March 3, 2011
BAG3-related myofibrillar myopathy in a Chinese family
H C Lee, S W Cherk, S K Chan, et al.
Clinical Genetics
|
February 26, 2011
Novel glucokinase mutations in patients with monogenic diabetes - clinical outline of GCK-MD and potential for founder effect in Slavic population
M Borowiec, K Antosik, W Fendler, et al.
Clinical Genetics
|
January 26, 2011
Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations
P C Johannesma, H M van der Klift, N C T van Grieken, et al.
Clinical Genetics
|
January 25, 2011
Clinical, biochemical and molecular characterization of cystinuria in a cohort of 12 patients
M Barbosa, A Lopes, C Mota, et al.
Page
of 718
Search research articles
Search
Showing results (671-680 of 7,173) with videos related to
Sort By:
Page
of 718
Clinical Genetics
|
April 19, 2011
Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformations
V Bhat, S C Girimaji, G Mohan, et al.
Clinical Genetics
|
June 24, 2011
Using Alzheimer's disease as a model for genetic risk disclosure: implications for personal genomics
J S Roberts, K D Christensen, R C Green
Clinical Genetics
|
June 24, 2011
Genotype-phenotype correlation in colorectal polyposis
K F Newton, E K L Mallinson, J Bowen, et al.
Clinical Genetics
|
December 16, 2010
Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome
L Raskin, F Schwenter, M Freytsis, et al.
Clinical Genetics
|
December 24, 2010
Congenital myasthenic syndrome associated with epidermolysis bullosa caused by homozygous mutations in PLEC1 and CHRNE
R A Maselli, J Arredondo, O Cagney, et al.
Clinical Genetics
|
January 5, 2011
Breast cancer after bilateral risk-reducing mastectomy
A-B Skytte, D Crüger, M Gerster, et al.
Clinical Genetics
|
March 3, 2011
BAG3-related myofibrillar myopathy in a Chinese family
H C Lee, S W Cherk, S K Chan, et al.
Clinical Genetics
|
February 26, 2011
Novel glucokinase mutations in patients with monogenic diabetes - clinical outline of GCK-MD and potential for founder effect in Slavic population
M Borowiec, K Antosik, W Fendler, et al.
Clinical Genetics
|
January 26, 2011
Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations
P C Johannesma, H M van der Klift, N C T van Grieken, et al.
Clinical Genetics
|
January 25, 2011
Clinical, biochemical and molecular characterization of cystinuria in a cohort of 12 patients
M Barbosa, A Lopes, C Mota, et al.
Page
of 718