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American Journal of Medical Genetics
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September 15, 1992
Deletion (14) (q24.3q32.1): evidence for a distinct clinical phenotype
S A Karnitis, K Burns, K W Sudduth, et al.
American Journal of Medical Genetics
|
October 1, 1989
Holoprosencephaly and interstitial deletion of 2(p2101p2109)
W G Wilson, D E Shanks, K W Sudduth, et al.
American Journal of Medical Genetics
|
November 1, 1987
Deletion (13)(q14.1q14.3) in two generations: variability of ocular manifestations and definition of the phenotype
W G Wilson, P A Campochiaro, B P Conway, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 3) with videos related to
Sort By:
Page
of 1
American Journal of Medical Genetics
|
September 15, 1992
Deletion (14) (q24.3q32.1): evidence for a distinct clinical phenotype
S A Karnitis, K Burns, K W Sudduth, et al.
American Journal of Medical Genetics
|
October 1, 1989
Holoprosencephaly and interstitial deletion of 2(p2101p2109)
W G Wilson, D E Shanks, K W Sudduth, et al.
American Journal of Medical Genetics
|
November 1, 1987
Deletion (13)(q14.1q14.3) in two generations: variability of ocular manifestations and definition of the phenotype
W G Wilson, P A Campochiaro, B P Conway, et al.
Page
of 1