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Skeletal Radiology
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February 1, 1997
Chiari malformation and tonsillar ectopia in twin brothers and father with autosomal dominant spondylo-epiphyseal dysplasia tarda
K W Gripp, C I Scott, L Nicholson, et al.
The Journal of Rheumatology
|
April 1, 1993
Inflammatory arthropathies in children with chromosomal abnormalities
D H Ihnat, G McIlvain-Simpson, K Conard, et al.
Developmental Medicine and Child Neurology
|
January 1, 1994
The spasmodic upper-body squeeze: a characteristic behavior in Smith-Magenis syndrome
B M Finucane, D Konar, B Haas-Givler, et al.
American Journal of Medical Genetics
|
February 15, 1993
Eye abnormalities in the Smith-Magenis contiguous gene deletion syndrome
B M Finucane, E R Jaeger, M B Kurtz, et al.
Humangenetik
|
January 1, 1973
Identification of a D-E(15-18) translocation chromosome by quinacrine fluorescence and urea banding techniques
D S Borgaonkar, L Ebenezer, C I Scott, et al.
American Journal of Medical Genetics
|
August 1, 1987
The Nager syndrome
J T Hecht, L L Immken, L F Harris, et al.
American Journal of Medical Genetics
|
May 3, 1996
Sponastrime dysplasia: five new cases and review of nine previously published cases
L O Langer, R K Beals, S LaFranchi, et al.
Annals of Neurology
|
January 1, 1980
Central core disease and malignant hyperthermia syndrome
J P Frank, Y Harati, I J Butler, et al.
American Journal of Medical Genetics
|
November 11, 1996
Extending the spectrum of distal arthrogryposis
K W Gripp, C I Scott, B C Brockett, et al.
American Journal of Medical Genetics. Part A
|
September 4, 2007
Weight for age charts for children with achondroplasia
J E Hoover-Fong, J McGready, K J Schulze, et al.
Page
of 12
Search research articles
Search
Showing results (71-80 of 116) with videos related to
Sort By:
Page
of 12
Skeletal Radiology
|
February 1, 1997
Chiari malformation and tonsillar ectopia in twin brothers and father with autosomal dominant spondylo-epiphyseal dysplasia tarda
K W Gripp, C I Scott, L Nicholson, et al.
The Journal of Rheumatology
|
April 1, 1993
Inflammatory arthropathies in children with chromosomal abnormalities
D H Ihnat, G McIlvain-Simpson, K Conard, et al.
Developmental Medicine and Child Neurology
|
January 1, 1994
The spasmodic upper-body squeeze: a characteristic behavior in Smith-Magenis syndrome
B M Finucane, D Konar, B Haas-Givler, et al.
American Journal of Medical Genetics
|
February 15, 1993
Eye abnormalities in the Smith-Magenis contiguous gene deletion syndrome
B M Finucane, E R Jaeger, M B Kurtz, et al.
Humangenetik
|
January 1, 1973
Identification of a D-E(15-18) translocation chromosome by quinacrine fluorescence and urea banding techniques
D S Borgaonkar, L Ebenezer, C I Scott, et al.
American Journal of Medical Genetics
|
August 1, 1987
The Nager syndrome
J T Hecht, L L Immken, L F Harris, et al.
American Journal of Medical Genetics
|
May 3, 1996
Sponastrime dysplasia: five new cases and review of nine previously published cases
L O Langer, R K Beals, S LaFranchi, et al.
Annals of Neurology
|
January 1, 1980
Central core disease and malignant hyperthermia syndrome
J P Frank, Y Harati, I J Butler, et al.
American Journal of Medical Genetics
|
November 11, 1996
Extending the spectrum of distal arthrogryposis
K W Gripp, C I Scott, B C Brockett, et al.
American Journal of Medical Genetics. Part A
|
September 4, 2007
Weight for age charts for children with achondroplasia
J E Hoover-Fong, J McGready, K J Schulze, et al.
Page
of 12