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Prenatal Diagnosis
|
August 18, 2006
Awareness and attitude toward prenatal diagnosis of chromosomal abnormalities in patients with no access to legal termination of pregnancy
E Gadow, F Petracchi, L Igarzabal, et al.
American Journal of Medical Genetics
|
December 5, 2000
Uruguay facio-cardio-musculo-skeletal syndrome: a novel X-linked recessive disorder
R Quadrelli, A Vaglio, S Reyno, et al.
Pediatric Dermatology
|
January 6, 1999
Van der Woude syndrome. A case report
R Vignale, J Araujo, G Pascal, et al.
Clinical Genetics
|
June 30, 2010
Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysis
V Grossmann, M Höckner, H Karmous-Benailly, et al.
Diseases of the Colon and Rectum
|
March 25, 2000
Hereditary nonpolyposis colorectal cancer (Lynch syndrome II) in Uruguay
C Sarroca, N Alfano, G T Bendin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 17, 1999
Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations
C T Basson, T Huang, R C Lin, et al.
Human Mutation
|
December 19, 2001
Nine novel mutations in NR0B1 (DAX1) causing adrenal hypoplasia congenita
Y H Zhang, B L Huang, K Anyane-Yeboa, et al.
Teratology
|
December 1, 1996
Thalidomide, a current teratogen in South America
E E Castilla, P Ashton-Prolla, E Barreda-Mejia, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Prenatal Diagnosis
|
August 18, 2006
Awareness and attitude toward prenatal diagnosis of chromosomal abnormalities in patients with no access to legal termination of pregnancy
E Gadow, F Petracchi, L Igarzabal, et al.
American Journal of Medical Genetics
|
December 5, 2000
Uruguay facio-cardio-musculo-skeletal syndrome: a novel X-linked recessive disorder
R Quadrelli, A Vaglio, S Reyno, et al.
Pediatric Dermatology
|
January 6, 1999
Van der Woude syndrome. A case report
R Vignale, J Araujo, G Pascal, et al.
Clinical Genetics
|
June 30, 2010
Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysis
V Grossmann, M Höckner, H Karmous-Benailly, et al.
Diseases of the Colon and Rectum
|
March 25, 2000
Hereditary nonpolyposis colorectal cancer (Lynch syndrome II) in Uruguay
C Sarroca, N Alfano, G T Bendin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 17, 1999
Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations
C T Basson, T Huang, R C Lin, et al.
Human Mutation
|
December 19, 2001
Nine novel mutations in NR0B1 (DAX1) causing adrenal hypoplasia congenita
Y H Zhang, B L Huang, K Anyane-Yeboa, et al.
Teratology
|
December 1, 1996
Thalidomide, a current teratogen in South America
E E Castilla, P Ashton-Prolla, E Barreda-Mejia, et al.
Page
of 1