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American Journal of Medical Genetics
|
February 13, 1995
Summary of the 1993 ASHG ancillary meeting "recent research on chromosome 4p syndromes and genes"
L L Estabrooks, W R Breg, M R Hayden, et al.
Nature Genetics
|
April 1, 1992
Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A
J R Lupski, C A Wise, A Kuwano, et al.
JAMA
|
January 17, 2023
Association of Supernumerary Sex Chromosome Aneuploidies With Venous Thromboembolism
Alexander S F Berry, Brenda M Finucane, Scott M Myers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 23, 2008
Enhanced detection of clinically relevant genomic imbalances using a targeted plus whole genome oligonucleotide microarray
Erin L Baldwin, Ji-Yun Lee, Douglas M Blake, et al.
The Journal of Biological Chemistry
|
January 25, 1988
Human hepatic lipase. Cloned cDNA sequence, restriction fragment length polymorphisms, chromosomal localization, and evolutionary relationships with lipoprotein lipase and pancreatic lipase
S Datta, C C Luo, W H Li, et al.
Genomics
|
August 1, 1990
The human homolog of murine Evi-2 lies between two von Recklinghausen neurofibromatosis translocations
P O'Connell, D Viskochil, A M Buchberg, et al.
Genetic Testing
|
January 1, 1997
Methylation analysis of the fragile X syndrome by PCR
S Das, T Kubota, M Song, et al.
Physical Review Letters
|
August 25, 2004
Monocrystal elastic constants of the negative-thermal-expansion compound zirconium tungstate (ZrW2O8)
F R Drymiotis, H Ledbetter, J B Betts, et al.
Journal of Personalized Medicine
|
June 2, 2021
Population Genomic Screening for Genetic Etiologies of Neurodevelopmental/Psychiatric Disorders Demonstrates Personal Utility and Positive Participant Responses
Karen E Wain, Kasia Tolwinski, Emily Palen, et al.
American Journal of Medical Genetics
|
September 15, 1994
A variety of genetic mechanisms are associated with the Prader-Willi syndrome
T Woodage, Z M Deng, M Prasad, et al.
Page
of 39
Search research articles
Search
Showing results (241-250 of 388) with videos related to
Sort By:
Page
of 39
American Journal of Medical Genetics
|
February 13, 1995
Summary of the 1993 ASHG ancillary meeting "recent research on chromosome 4p syndromes and genes"
L L Estabrooks, W R Breg, M R Hayden, et al.
Nature Genetics
|
April 1, 1992
Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A
J R Lupski, C A Wise, A Kuwano, et al.
JAMA
|
January 17, 2023
Association of Supernumerary Sex Chromosome Aneuploidies With Venous Thromboembolism
Alexander S F Berry, Brenda M Finucane, Scott M Myers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 23, 2008
Enhanced detection of clinically relevant genomic imbalances using a targeted plus whole genome oligonucleotide microarray
Erin L Baldwin, Ji-Yun Lee, Douglas M Blake, et al.
The Journal of Biological Chemistry
|
January 25, 1988
Human hepatic lipase. Cloned cDNA sequence, restriction fragment length polymorphisms, chromosomal localization, and evolutionary relationships with lipoprotein lipase and pancreatic lipase
S Datta, C C Luo, W H Li, et al.
Genomics
|
August 1, 1990
The human homolog of murine Evi-2 lies between two von Recklinghausen neurofibromatosis translocations
P O'Connell, D Viskochil, A M Buchberg, et al.
Genetic Testing
|
January 1, 1997
Methylation analysis of the fragile X syndrome by PCR
S Das, T Kubota, M Song, et al.
Physical Review Letters
|
August 25, 2004
Monocrystal elastic constants of the negative-thermal-expansion compound zirconium tungstate (ZrW2O8)
F R Drymiotis, H Ledbetter, J B Betts, et al.
Journal of Personalized Medicine
|
June 2, 2021
Population Genomic Screening for Genetic Etiologies of Neurodevelopmental/Psychiatric Disorders Demonstrates Personal Utility and Positive Participant Responses
Karen E Wain, Kasia Tolwinski, Emily Palen, et al.
American Journal of Medical Genetics
|
September 15, 1994
A variety of genetic mechanisms are associated with the Prader-Willi syndrome
T Woodage, Z M Deng, M Prasad, et al.
Page
of 39