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Matrix Biology : Journal of the International Society for Matrix Biology
|
November 20, 1998
Proteoglycan sulfation in cartilage and cell cultures from patients with sulfate transporter chondrodysplasias: relationship to clinical severity and indications on the role of intracellular sulfate production
A Rossi, I Kaitila, W R Wilcox, et al.
Diabetes
|
February 1, 1983
HLA genotypic study of insulin-dependent diabetes the excess of DR3/DR4 heterozygotes allows rejection of the recessive hypothesis
J I Rotter, C E Anderson, R Rubin, et al.
The New England Journal of Medicine
|
October 1, 1970
Endochondral ossification in achondroplastic dwarfism
D L Rimoin, G N Hughes, R L Kaufman, et al.
American Journal of Medical Genetics
|
November 1, 1982
Spondylometepiphyseal dysplasia, Strudwick type
C E Anderson, D O Sillence, R S Lachman, et al.
American Journal of Medical Genetics
|
March 27, 1995
Bilateral ulna hypoplasia, club feet, and mental retardation: a new mesomelic syndrome
G Kohn, G Malinger, R el Shawwa, et al.
American Journal of Medical Genetics
|
February 1, 1985
Oto-palato-digital syndrome, type II--an X-linked skeletal dysplasia
T G Brewster, R S Lachman, D C Kushner, et al.
Prenatal Diagnosis
|
May 18, 1999
Prenatal diagnosis of rhizomelic chondrodysplasia punctata due to isolated alkyldihydroacetonephosphate acyltransferase synthase deficiency
K M Brookhyser, M H Lipson, A B Moser, et al.
The Journal of Pediatrics
|
May 1, 1974
The Winchester syndrome: a nonlysosomal connective tissue disease
D W Hollister, D L Rimoin, R S Lachman, et al.
American Journal of Medical Genetics
|
January 2, 1996
Epidemiology of osteochondrodysplasias: changing trends due to advances in prenatal diagnosis
S A Rasmussen, F R Bieber, B R Benacerraf, et al.
American Journal of Ophthalmology
|
February 1, 1984
Leber's congenital amaurosis associated with familial juvenile nephronophthisis and cone-shaped epiphyses of the hands (the Saldino-Mainzer syndrome)
D S Ellis, J R Heckenlively, C L Martin, et al.
Page
of 29
Search research articles
Search
Showing results (201-210 of 284) with videos related to
Sort By:
Page
of 29
Matrix Biology : Journal of the International Society for Matrix Biology
|
November 20, 1998
Proteoglycan sulfation in cartilage and cell cultures from patients with sulfate transporter chondrodysplasias: relationship to clinical severity and indications on the role of intracellular sulfate production
A Rossi, I Kaitila, W R Wilcox, et al.
Diabetes
|
February 1, 1983
HLA genotypic study of insulin-dependent diabetes the excess of DR3/DR4 heterozygotes allows rejection of the recessive hypothesis
J I Rotter, C E Anderson, R Rubin, et al.
The New England Journal of Medicine
|
October 1, 1970
Endochondral ossification in achondroplastic dwarfism
D L Rimoin, G N Hughes, R L Kaufman, et al.
American Journal of Medical Genetics
|
November 1, 1982
Spondylometepiphyseal dysplasia, Strudwick type
C E Anderson, D O Sillence, R S Lachman, et al.
American Journal of Medical Genetics
|
March 27, 1995
Bilateral ulna hypoplasia, club feet, and mental retardation: a new mesomelic syndrome
G Kohn, G Malinger, R el Shawwa, et al.
American Journal of Medical Genetics
|
February 1, 1985
Oto-palato-digital syndrome, type II--an X-linked skeletal dysplasia
T G Brewster, R S Lachman, D C Kushner, et al.
Prenatal Diagnosis
|
May 18, 1999
Prenatal diagnosis of rhizomelic chondrodysplasia punctata due to isolated alkyldihydroacetonephosphate acyltransferase synthase deficiency
K M Brookhyser, M H Lipson, A B Moser, et al.
The Journal of Pediatrics
|
May 1, 1974
The Winchester syndrome: a nonlysosomal connective tissue disease
D W Hollister, D L Rimoin, R S Lachman, et al.
American Journal of Medical Genetics
|
January 2, 1996
Epidemiology of osteochondrodysplasias: changing trends due to advances in prenatal diagnosis
S A Rasmussen, F R Bieber, B R Benacerraf, et al.
American Journal of Ophthalmology
|
February 1, 1984
Leber's congenital amaurosis associated with familial juvenile nephronophthisis and cone-shaped epiphyses of the hands (the Saldino-Mainzer syndrome)
D S Ellis, J R Heckenlively, C L Martin, et al.
Page
of 29