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Clinical Genetics
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February 1, 1995
Split foot and developmental retardation associated with a deletion of three microsatellite markers in 7q21.2-q22.1
J C Marinoni, R E Stevenson, J P Evans, et al.
Clinical Genetics
|
May 8, 2009
Escape of the yolk sac: a hypothesis to explain the embryogenesis of gastroschisis
R E Stevenson, R C Rogers, J C Chandler, et al.
American Journal of Medical Genetics. Part A
|
June 15, 2007
Pelizaeus-Merzbacher syndrome: neurocognitive function in a family with carrier manifestations
Michael Marble, Kytja S Voeller, Melanie M May, et al.
American Journal of Medical Genetics. Part A
|
September 19, 2009
Partial ATRX gene duplication causes ATR-X syndrome
Dianne M Cohn, Roberta A Pagon, Louanne Hudgins, et al.
Clinical Dysmorphology
|
November 14, 2021
Angelman syndrome with a 15q11q13 deletion in a mother and daughter
Shannon Bell, Kameryn M Butler, Kathryn T Drazba, et al.
British Medical Journal
|
September 9, 1978
Effect of stopping low-phenylalanine diet on intellectual progress of children with phenylketonuria
I Smith, M E Lobascher, J E Stevenson, et al.
American Journal of Medical Genetics
|
July 9, 1999
XLMR database
D A Cabezas, J F Arena, R E Stevenson, et al.
Cell Genomics
|
December 5, 2024
Adult single-nucleus neuronal transcriptomes of insulin signaling mutants reveal regulators of behavior and learning
Jonathan St Ange, Yifei Weng, Rachel Kaletsky, et al.
Environmental Pollution (Barking, Essex : 1987)
|
May 26, 2007
Ozone uptake (flux) as it relates to ozone-induced foliar symptoms of Prunus serotina and Populus maximowiziixtrichocarpa
T Orendovici-Best, J M Skelly, D D Davis, et al.
Journal of Medical Genetics
|
June 1, 1997
Arch fingerprints, hypotonia, and areflexia associated with X linked mental retardation
R E Stevenson, B Häne, J F Arena, et al.
Page
of 67
Search research articles
Search
Showing results (331-340 of 665) with videos related to
Sort By:
Page
of 67
Clinical Genetics
|
February 1, 1995
Split foot and developmental retardation associated with a deletion of three microsatellite markers in 7q21.2-q22.1
J C Marinoni, R E Stevenson, J P Evans, et al.
Clinical Genetics
|
May 8, 2009
Escape of the yolk sac: a hypothesis to explain the embryogenesis of gastroschisis
R E Stevenson, R C Rogers, J C Chandler, et al.
American Journal of Medical Genetics. Part A
|
June 15, 2007
Pelizaeus-Merzbacher syndrome: neurocognitive function in a family with carrier manifestations
Michael Marble, Kytja S Voeller, Melanie M May, et al.
American Journal of Medical Genetics. Part A
|
September 19, 2009
Partial ATRX gene duplication causes ATR-X syndrome
Dianne M Cohn, Roberta A Pagon, Louanne Hudgins, et al.
Clinical Dysmorphology
|
November 14, 2021
Angelman syndrome with a 15q11q13 deletion in a mother and daughter
Shannon Bell, Kameryn M Butler, Kathryn T Drazba, et al.
British Medical Journal
|
September 9, 1978
Effect of stopping low-phenylalanine diet on intellectual progress of children with phenylketonuria
I Smith, M E Lobascher, J E Stevenson, et al.
American Journal of Medical Genetics
|
July 9, 1999
XLMR database
D A Cabezas, J F Arena, R E Stevenson, et al.
Cell Genomics
|
December 5, 2024
Adult single-nucleus neuronal transcriptomes of insulin signaling mutants reveal regulators of behavior and learning
Jonathan St Ange, Yifei Weng, Rachel Kaletsky, et al.
Environmental Pollution (Barking, Essex : 1987)
|
May 26, 2007
Ozone uptake (flux) as it relates to ozone-induced foliar symptoms of Prunus serotina and Populus maximowiziixtrichocarpa
T Orendovici-Best, J M Skelly, D D Davis, et al.
Journal of Medical Genetics
|
June 1, 1997
Arch fingerprints, hypotonia, and areflexia associated with X linked mental retardation
R E Stevenson, B Häne, J F Arena, et al.
Page
of 67