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Clinical Genetics
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January 1, 1991
Dizygotic twins concordant for truncus arteriosus
M J Lang, D J Aughton, T W Riggs, et al.
BMC Medical Genetics
|
October 25, 2008
Extending the spectrum of Ellis van Creveld syndrome: a large family with a mild mutation in the EVC gene
Hakan Ulucan, Davut Gül, Julie C Sapp, et al.
The Journal of Clinical Investigation
|
November 9, 2000
A GNAS1 imprinting defect in pseudohypoparathyroidism type IB
J Liu, D Litman, M J Rosenberg, et al.
Journal of Pediatric Surgery
|
June 22, 2002
Principles for the surgical management of patients with Proteus syndrome and patients with overgrowth not meeting Proteus criteria
Matthew Lublin, Douglas J Schwartzentruber, Jeff Lukish, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 19, 2010
Validation of My Family Health Portrait for six common heritable conditions
Flavia M Facio, W Gregory Feero, Amy Linn, et al.
European Journal of Human Genetics : EJHG
|
July 7, 2011
Motivators for participation in a whole-genome sequencing study: implications for translational genomics research
Flavia M Facio, Stephanie Brooks, Johanna Loewenstein, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
November 7, 2019
A dyadic genotype-phenotype approach to diagnostic criteria for Proteus syndrome
Julie C Sapp, Anna Buser, Jasmine Burton-Akright, et al.
Journal of the American Academy of Dermatology
|
February 10, 2020
Hypertrichotic patches as a mosaic manifestation of Proteus syndrome
Deeti J Pithadia, John W Roman, Julie C Sapp, et al.
The Journal of Pediatrics
|
December 1, 1993
Autosomal dominant transmission of the Pallister-Hall syndrome
K F Topf, G B Kletter, R P Kelch, et al.
Transplantation Proceedings
|
February 1, 1989
Inflammatory mediators in allograft malfunction: a new concept in the cyclosporin era
S M Katz, S M Greenstein, S Simonian, et al.
Page
of 48
Search research articles
Search
Showing results (191-200 of 475) with videos related to
Sort By:
Page
of 48
Clinical Genetics
|
January 1, 1991
Dizygotic twins concordant for truncus arteriosus
M J Lang, D J Aughton, T W Riggs, et al.
BMC Medical Genetics
|
October 25, 2008
Extending the spectrum of Ellis van Creveld syndrome: a large family with a mild mutation in the EVC gene
Hakan Ulucan, Davut Gül, Julie C Sapp, et al.
The Journal of Clinical Investigation
|
November 9, 2000
A GNAS1 imprinting defect in pseudohypoparathyroidism type IB
J Liu, D Litman, M J Rosenberg, et al.
Journal of Pediatric Surgery
|
June 22, 2002
Principles for the surgical management of patients with Proteus syndrome and patients with overgrowth not meeting Proteus criteria
Matthew Lublin, Douglas J Schwartzentruber, Jeff Lukish, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 19, 2010
Validation of My Family Health Portrait for six common heritable conditions
Flavia M Facio, W Gregory Feero, Amy Linn, et al.
European Journal of Human Genetics : EJHG
|
July 7, 2011
Motivators for participation in a whole-genome sequencing study: implications for translational genomics research
Flavia M Facio, Stephanie Brooks, Johanna Loewenstein, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
November 7, 2019
A dyadic genotype-phenotype approach to diagnostic criteria for Proteus syndrome
Julie C Sapp, Anna Buser, Jasmine Burton-Akright, et al.
Journal of the American Academy of Dermatology
|
February 10, 2020
Hypertrichotic patches as a mosaic manifestation of Proteus syndrome
Deeti J Pithadia, John W Roman, Julie C Sapp, et al.
The Journal of Pediatrics
|
December 1, 1993
Autosomal dominant transmission of the Pallister-Hall syndrome
K F Topf, G B Kletter, R P Kelch, et al.
Transplantation Proceedings
|
February 1, 1989
Inflammatory mediators in allograft malfunction: a new concept in the cyclosporin era
S M Katz, S M Greenstein, S Simonian, et al.
Page
of 48