Search research articles
Contact Us
Filters
Showing results (691-700 of 2,367) with videos related to
Page
of 237
Sort By:
Human Heredity
|
February 17, 1998
Linkage of autosomal recessive primary congenital glaucoma to the GLC3A locus in Roms (Gypsies) from Slovakia
M Plásilová, E Feráková, L Kádasi, et al.
Human Heredity
|
January 1, 1976
Saliva acid phosphatases: genetic studies
S G Tan, G C Ashton
Human Heredity
|
April 4, 1998
Screening 25 dystrophin gene exons for deletions in Arab children with Duchenne muscular dystrophy
M Z Haider, L Bastaki, Y Habib, et al.
Human Heredity
|
April 4, 1998
Fluorescence in situ hybridization of psu dic(X)(Xpter-Xq21::Xq21-Xpter) in two patients with Turner's syndrome
R Fernández, E Pásaro
Human Heredity
|
April 4, 1998
G6PD variants in three South American ethnic groups: population distribution and description of two new mutations
T A Weimer, F M Salzano, B Westwood, et al.
Human Heredity
|
November 14, 2003
Haplotype frequency estimation in the presence of genotyping errors
Guohua Zou, Hongyu Zhao
Human Heredity
|
January 1, 1992
Characterization of a 28-kD polymorphic polypeptide detected by two-dimensional electrophoresis of human platelets
S Iwamoto, E Kajii, T Omi, et al.
Human Heredity
|
January 1, 1992
Effective population size of a rural village on a large plain (Veggiano, Padua, Italy)
S Presciuttini, G U Caravello, A Baroni
Human Heredity
|
January 1, 1992
Deletional types of alpha-thalassaemia in central Java
J A Tan, J S Tay, A Soemantri, et al.
Human Heredity
|
January 1, 1992
Type II hereditary angio-oedema associated with two mutations in one allele of the C1-inhibitor gene around the reactive-site coding region
Z Siddique, A R McPhaden, K Whaley
Page
of 237
Search research articles
Search
Showing results (691-700 of 2,367) with videos related to
Sort By:
Page
of 237
Human Heredity
|
February 17, 1998
Linkage of autosomal recessive primary congenital glaucoma to the GLC3A locus in Roms (Gypsies) from Slovakia
M Plásilová, E Feráková, L Kádasi, et al.
Human Heredity
|
January 1, 1976
Saliva acid phosphatases: genetic studies
S G Tan, G C Ashton
Human Heredity
|
April 4, 1998
Screening 25 dystrophin gene exons for deletions in Arab children with Duchenne muscular dystrophy
M Z Haider, L Bastaki, Y Habib, et al.
Human Heredity
|
April 4, 1998
Fluorescence in situ hybridization of psu dic(X)(Xpter-Xq21::Xq21-Xpter) in two patients with Turner's syndrome
R Fernández, E Pásaro
Human Heredity
|
April 4, 1998
G6PD variants in three South American ethnic groups: population distribution and description of two new mutations
T A Weimer, F M Salzano, B Westwood, et al.
Human Heredity
|
November 14, 2003
Haplotype frequency estimation in the presence of genotyping errors
Guohua Zou, Hongyu Zhao
Human Heredity
|
January 1, 1992
Characterization of a 28-kD polymorphic polypeptide detected by two-dimensional electrophoresis of human platelets
S Iwamoto, E Kajii, T Omi, et al.
Human Heredity
|
January 1, 1992
Effective population size of a rural village on a large plain (Veggiano, Padua, Italy)
S Presciuttini, G U Caravello, A Baroni
Human Heredity
|
January 1, 1992
Deletional types of alpha-thalassaemia in central Java
J A Tan, J S Tay, A Soemantri, et al.
Human Heredity
|
January 1, 1992
Type II hereditary angio-oedema associated with two mutations in one allele of the C1-inhibitor gene around the reactive-site coding region
Z Siddique, A R McPhaden, K Whaley
Page
of 237