Search research articles
Contact Us
Filters
Showing results (1-10 of 4) with videos related to
Page
of 1
Sort By:
American Journal of Medical Genetics
|
February 27, 2001
46,XX gonadal dysgenesis, short stature, and recurrent metabolic acidosis in two sisters
F M Hisama, S Zemel, E M Cherniske, et al.
Clinical Dysmorphology
|
May 13, 1999
Early puberty in Williams syndrome
E M Cherniske, L S Sadler, D Schwartz, et al.
Human Molecular Genetics
|
May 24, 2001
Truncating mutations in FOXC2 cause multiple lymphedema syndromes
D N Finegold, M A Kimak, E C Lawrence, et al.
Journal of Medical Genetics
|
May 23, 1998
Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?
J J Jonsson, A Renieri, P G Gallagher, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 4) with videos related to
Sort By:
Page
of 1
American Journal of Medical Genetics
|
February 27, 2001
46,XX gonadal dysgenesis, short stature, and recurrent metabolic acidosis in two sisters
F M Hisama, S Zemel, E M Cherniske, et al.
Clinical Dysmorphology
|
May 13, 1999
Early puberty in Williams syndrome
E M Cherniske, L S Sadler, D Schwartz, et al.
Human Molecular Genetics
|
May 24, 2001
Truncating mutations in FOXC2 cause multiple lymphedema syndromes
D N Finegold, M A Kimak, E C Lawrence, et al.
Journal of Medical Genetics
|
May 23, 1998
Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?
J J Jonsson, A Renieri, P G Gallagher, et al.
Page
of 1