Search research articles
Contact Us
Filters
Showing results (1181-1190 of 9,569) with videos related to
Page
of 957
Sort By:
Human Genetics
|
January 1, 1983
Some genetic implications of isoelectric focusing of human red cell phosphoglucomutase (PGM1) and serum protein group specific component (Gc): genetic diversity in the populations of Himachal Pradesh, India
S S Papiha, I White, D F Roberts
Human Genetics
|
January 1, 1982
Human chromosomal polymorphism. IV. Chromosomal Q polymorphism in Russians living in Kirghizia
A I Ibraimov, M M Mirrakhimov
Human Genetics
|
January 1, 1983
Down's syndrome in the male. Reproductive pathology and meiotic studies
R Johannisson, A Gropp, H Winking, et al.
Human Genetics
|
January 1, 1979
An uncommon phenotypical variant in the Shereshevsky-Turner syndrome
I G Dzenis, N N Antipina
Human Genetics
|
January 1, 1979
Omphalocele and partial trisomy 1q syndrome
H Chen, J J Gershanik, J B Mailhes, et al.
Human Genetics
|
January 1, 1979
H-Y antigen in Swyer syndrome and the genetics of XY gonadal dysgenesis
C A Moreira-Filho, S P Toledo, V R Bagnolli, et al.
Human Genetics
|
January 25, 1979
Trisomy 12p syndrome: de novo occurrence of mosaic trisomy 12p in a mentally retarded boy
I Kondo, H Hamaguchi, T Haneda
Human Genetics
|
January 25, 1979
Translocation C:D involving chromosomes 11 and 14
M H Callow, A R Boon, E V Davison
Human Genetics
|
September 6, 2022
Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes-Brocks syndrome 2
Anne Christians, Esra Kesdiren, Imke Hennies, et al.
Human Genetics
|
November 1, 1986
Complex chromosomal rearrangement and multiple spontaneous abortions
J L Gorski, B S Emanuel, E H Zackai, et al.
Page
of 957
Search research articles
Search
Showing results (1181-1190 of 9,569) with videos related to
Sort By:
Page
of 957
Human Genetics
|
January 1, 1983
Some genetic implications of isoelectric focusing of human red cell phosphoglucomutase (PGM1) and serum protein group specific component (Gc): genetic diversity in the populations of Himachal Pradesh, India
S S Papiha, I White, D F Roberts
Human Genetics
|
January 1, 1982
Human chromosomal polymorphism. IV. Chromosomal Q polymorphism in Russians living in Kirghizia
A I Ibraimov, M M Mirrakhimov
Human Genetics
|
January 1, 1983
Down's syndrome in the male. Reproductive pathology and meiotic studies
R Johannisson, A Gropp, H Winking, et al.
Human Genetics
|
January 1, 1979
An uncommon phenotypical variant in the Shereshevsky-Turner syndrome
I G Dzenis, N N Antipina
Human Genetics
|
January 1, 1979
Omphalocele and partial trisomy 1q syndrome
H Chen, J J Gershanik, J B Mailhes, et al.
Human Genetics
|
January 1, 1979
H-Y antigen in Swyer syndrome and the genetics of XY gonadal dysgenesis
C A Moreira-Filho, S P Toledo, V R Bagnolli, et al.
Human Genetics
|
January 25, 1979
Trisomy 12p syndrome: de novo occurrence of mosaic trisomy 12p in a mentally retarded boy
I Kondo, H Hamaguchi, T Haneda
Human Genetics
|
January 25, 1979
Translocation C:D involving chromosomes 11 and 14
M H Callow, A R Boon, E V Davison
Human Genetics
|
September 6, 2022
Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes-Brocks syndrome 2
Anne Christians, Esra Kesdiren, Imke Hennies, et al.
Human Genetics
|
November 1, 1986
Complex chromosomal rearrangement and multiple spontaneous abortions
J L Gorski, B S Emanuel, E H Zackai, et al.
Page
of 957