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American Journal of Human Genetics
|
September 1, 1987
Localization of the human thyroxine-binding globulin gene to the long arm of the X chromosome (Xq21-22)
J M Trent, I L Flink, E Morkin, et al.
American Journal of Human Genetics
|
March 1, 1991
Clinical and molecular diagnosis of Miller-Dieker syndrome
W B Dobyns, C J Curry, H E Hoyme, et al.
Human Molecular Genetics
|
May 20, 1999
Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13)
S L Christian, J A Fantes, S K Mewborn, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
April 23, 2023
Letter to the editor
Brenda Finucane, Scott M Myers, Thomas D Challman, et al.
Molecular Medicine Today
|
June 22, 2000
Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis
R J Leventer, D T Pilz, N Matsumoto, et al.
JAMA Psychiatry
|
January 29, 2016
A Cross-Disorder Method to Identify Novel Candidate Genes for Developmental Brain Disorders
Andrea J Gonzalez-Mantilla, Andres Moreno-De-Luca, David H Ledbetter, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1986
Molecular cloning and chromosomal localization of human 4-beta-galactosyltransferase
M G Humphreys-Beher, B Bunnell, P vanTuinen, et al.
Somatic Cell and Molecular Genetics
|
May 1, 1986
Human liver fatty acid binding protein gene is located on chromosome 2
S H Chen, P Van Tuinen, D H Ledbetter, et al.
American Journal of Medical Genetics
|
January 1, 1990
A de novo X;3 translocation in Rett syndrome
H Y Zoghbi, D H Ledbetter, R Schultz, et al.
Genomics
|
July 1, 1995
The human corticotropin-releasing factor receptor (CRHR) gene maps to chromosome 17q12-q22
M H Polymeropoulos, R Torres, J A Yanovski, et al.
Page
of 39
Search research articles
Search
Showing results (121-130 of 388) with videos related to
Sort By:
Page
of 39
American Journal of Human Genetics
|
September 1, 1987
Localization of the human thyroxine-binding globulin gene to the long arm of the X chromosome (Xq21-22)
J M Trent, I L Flink, E Morkin, et al.
American Journal of Human Genetics
|
March 1, 1991
Clinical and molecular diagnosis of Miller-Dieker syndrome
W B Dobyns, C J Curry, H E Hoyme, et al.
Human Molecular Genetics
|
May 20, 1999
Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13)
S L Christian, J A Fantes, S K Mewborn, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
April 23, 2023
Letter to the editor
Brenda Finucane, Scott M Myers, Thomas D Challman, et al.
Molecular Medicine Today
|
June 22, 2000
Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis
R J Leventer, D T Pilz, N Matsumoto, et al.
JAMA Psychiatry
|
January 29, 2016
A Cross-Disorder Method to Identify Novel Candidate Genes for Developmental Brain Disorders
Andrea J Gonzalez-Mantilla, Andres Moreno-De-Luca, David H Ledbetter, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1986
Molecular cloning and chromosomal localization of human 4-beta-galactosyltransferase
M G Humphreys-Beher, B Bunnell, P vanTuinen, et al.
Somatic Cell and Molecular Genetics
|
May 1, 1986
Human liver fatty acid binding protein gene is located on chromosome 2
S H Chen, P Van Tuinen, D H Ledbetter, et al.
American Journal of Medical Genetics
|
January 1, 1990
A de novo X;3 translocation in Rett syndrome
H Y Zoghbi, D H Ledbetter, R Schultz, et al.
Genomics
|
July 1, 1995
The human corticotropin-releasing factor receptor (CRHR) gene maps to chromosome 17q12-q22
M H Polymeropoulos, R Torres, J A Yanovski, et al.
Page
of 39