Search research articles
Contact Us
Filters
Showing results (81-90 of 86) with videos related to
Page
of 9
Sort By:
You have reached the last page of results.
This site can display upto 86 results.
Pathologica
|
July 1, 1988
[Cloverleaf skull. Description of 4 cases]
G Camera, D Clerici Bagozzi, M G Salmoiraghi, et al.
Human Genetics
|
January 1, 1981
Expression of GALT in two unrelated 9p- patients. Evidence for assignment of the GALT locus to the 9p21 band
F Dagna Bricarelli, M Magnani, A Arslanian, et al.
Biochemical and Molecular Medicine
|
February 12, 1998
Phenotypic comparison of an osteogenesis imperfecta type IV proband with a de novo alpha2(I) Gly922 --> Ser substitution in type I collagen and an unrelated patient with an identical mutation
A Forlino, E D'amato, M Valli, et al.
American Journal of Medical Genetics
|
December 4, 1995
Hydrocephalus, skeletal anomalies, and mental disturbances in a mother and three daughters: a new syndrome
A Ferlini, M Ragno, P Gobbi, et al.
Journal of Medical Genetics
|
February 27, 2004
Acropectorovertebral dysgenesis (F syndrome) maps to chromosome 2q36
H Thiele, C McCann, S van't Padje, et al.
CNS Drugs
|
June 28, 2018
Atypical Post-Injection Reactions with Delayed Onset Following Glatiramer Acetate 40 mg: Need for Titration?
Chiara Zecca, G Bellavia, L Brambilla, et al.
Page
of 9
Search research articles
Search
Showing results (81-90 of 86) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 86 results.
Pathologica
|
July 1, 1988
[Cloverleaf skull. Description of 4 cases]
G Camera, D Clerici Bagozzi, M G Salmoiraghi, et al.
Human Genetics
|
January 1, 1981
Expression of GALT in two unrelated 9p- patients. Evidence for assignment of the GALT locus to the 9p21 band
F Dagna Bricarelli, M Magnani, A Arslanian, et al.
Biochemical and Molecular Medicine
|
February 12, 1998
Phenotypic comparison of an osteogenesis imperfecta type IV proband with a de novo alpha2(I) Gly922 --> Ser substitution in type I collagen and an unrelated patient with an identical mutation
A Forlino, E D'amato, M Valli, et al.
American Journal of Medical Genetics
|
December 4, 1995
Hydrocephalus, skeletal anomalies, and mental disturbances in a mother and three daughters: a new syndrome
A Ferlini, M Ragno, P Gobbi, et al.
Journal of Medical Genetics
|
February 27, 2004
Acropectorovertebral dysgenesis (F syndrome) maps to chromosome 2q36
H Thiele, C McCann, S van't Padje, et al.
CNS Drugs
|
June 28, 2018
Atypical Post-Injection Reactions with Delayed Onset Following Glatiramer Acetate 40 mg: Need for Titration?
Chiara Zecca, G Bellavia, L Brambilla, et al.
Page
of 9