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Genomics
|
April 1, 1997
Structure and organization of GABRB3 and GABRA5
K Glatt, H Glatt, M Lalande
Genomics
|
January 1, 1994
The human gamma-aminobutyric acid receptor subunit beta 3 and alpha 5 gene cluster in chromosome 15q11-q13 is rich in highly polymorphic (CA)n repeats
K Glatt, D Sinnett, M Lalande
Nucleic Acids Research
|
December 11, 1989
RFLPs for beta 2-microglobulin
R D Nicholls, K Glatt, S A Latt
Genomics
|
October 27, 1998
Characterization of two novel protocadherins (PCDH8 and PCDH9) localized on human chromosome 13 and mouse chromosome 14
S Strehl, K Glatt, Q M Liu, et al.
American Journal of Human Genetics
|
June 1, 1993
High-resolution mapping of the gamma-aminobutyric acid receptor subunit beta 3 and alpha 5 gene cluster on chromosome 15q11-q13, and localization of breakpoints in two Angelman syndrome patients
D Sinnett, J Wagstaff, K Glatt, et al.
American Journal of Human Genetics
|
December 1, 1989
Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP
M Simon, M Phillips, H Green, et al.
American Journal of Human Genetics
|
July 11, 1990
Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers
J H Knoll, R D Nicholls, R E Magenis, et al.
Human Molecular Genetics
|
February 1, 1993
FISH ordering of reference markers and of the gene for the alpha 5 subunit of the gamma-aminobutyric acid receptor (GABRA5) within the Angelman and Prader-Willi syndrome chromosomal regions
J H Knoll, D Sinnett, J Wagstaff, et al.
Gene
|
September 16, 1996
Identification of a putative DNA replication origin in the gamma-aminobutyric acid receptor subunit beta3 and alpha5 gene cluster on human chromosome 15q11-q13, a region associated with parental imprinting and allele-specific replication timing
D Sinnett, E Woolf, W Xie, et al.
American Journal of Medical Genetics
|
May 1, 1989
Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome
R D Nicholls, J H Knoll, K Glatt, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Genomics
|
April 1, 1997
Structure and organization of GABRB3 and GABRA5
K Glatt, H Glatt, M Lalande
Genomics
|
January 1, 1994
The human gamma-aminobutyric acid receptor subunit beta 3 and alpha 5 gene cluster in chromosome 15q11-q13 is rich in highly polymorphic (CA)n repeats
K Glatt, D Sinnett, M Lalande
Nucleic Acids Research
|
December 11, 1989
RFLPs for beta 2-microglobulin
R D Nicholls, K Glatt, S A Latt
Genomics
|
October 27, 1998
Characterization of two novel protocadherins (PCDH8 and PCDH9) localized on human chromosome 13 and mouse chromosome 14
S Strehl, K Glatt, Q M Liu, et al.
American Journal of Human Genetics
|
June 1, 1993
High-resolution mapping of the gamma-aminobutyric acid receptor subunit beta 3 and alpha 5 gene cluster on chromosome 15q11-q13, and localization of breakpoints in two Angelman syndrome patients
D Sinnett, J Wagstaff, K Glatt, et al.
American Journal of Human Genetics
|
December 1, 1989
Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP
M Simon, M Phillips, H Green, et al.
American Journal of Human Genetics
|
July 11, 1990
Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers
J H Knoll, R D Nicholls, R E Magenis, et al.
Human Molecular Genetics
|
February 1, 1993
FISH ordering of reference markers and of the gene for the alpha 5 subunit of the gamma-aminobutyric acid receptor (GABRA5) within the Angelman and Prader-Willi syndrome chromosomal regions
J H Knoll, D Sinnett, J Wagstaff, et al.
Gene
|
September 16, 1996
Identification of a putative DNA replication origin in the gamma-aminobutyric acid receptor subunit beta3 and alpha5 gene cluster on human chromosome 15q11-q13, a region associated with parental imprinting and allele-specific replication timing
D Sinnett, E Woolf, W Xie, et al.
American Journal of Medical Genetics
|
May 1, 1989
Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome
R D Nicholls, J H Knoll, K Glatt, et al.
Page
of 2