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American Journal of Medical Genetics
|
June 1, 1990
Atelosteogenesis type III: a distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digital syndrome type II
H J Stern, J M Graham, R S Lachman, et al.
American Journal of Human Genetics
|
March 31, 2000
Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene
L B Meira, J M Graham, C R Greenberg, et al.
Clinical Genetics
|
July 9, 2013
Phenotype-genotype correlations in patients with Marinesco-Sjögren syndrome
F Ezgu, P Krejci, S Li, et al.
Genomics
|
August 11, 1992
Deletion mapping of H-Y antigen to the long arm of the human Y chromosome
M A Cantrell, J S Bogan, E Simpson, et al.
American Journal of Medical Genetics
|
June 28, 2001
Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3
D N Schweitzer, J M Graham, R S Lachman, et al.
European Journal of Clinical Investigation
|
March 19, 2003
Effects of insulin lispro and chronic vitamin C therapy on postprandial lipaemia, oxidative stress and endothelial function in patients with type 2 diabetes mellitus
M Evans, R A Anderson, J C Smith, et al.
Neurology
|
December 15, 2004
Diffusion tensor imaging for the assessment of upper motor neuron integrity in ALS
J M Graham, N Papadakis, J Evans, et al.
American Journal of Medical Genetics
|
October 2, 1996
Report from the workshop on Pallister-Hall syndrome and related phenotypes
L G Biesecker, M Abbott, J Allen, et al.
Journal of Medical Genetics
|
January 15, 2003
P63 mutations are not a major cause of non-syndromic split hand/foot malformation
X J de Mollerat, D B Everman, C T Morgan, et al.
American Journal of Human Genetics
|
March 1, 1996
FGFR2 exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: evidence for missense changes, insertions, and a deletion due to alternative RNA splicing
G A Meyers, D Day, R Goldberg, et al.
Page
of 36
Search research articles
Search
Showing results (341-350 of 360) with videos related to
Sort By:
Page
of 36
American Journal of Medical Genetics
|
June 1, 1990
Atelosteogenesis type III: a distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digital syndrome type II
H J Stern, J M Graham, R S Lachman, et al.
American Journal of Human Genetics
|
March 31, 2000
Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene
L B Meira, J M Graham, C R Greenberg, et al.
Clinical Genetics
|
July 9, 2013
Phenotype-genotype correlations in patients with Marinesco-Sjögren syndrome
F Ezgu, P Krejci, S Li, et al.
Genomics
|
August 11, 1992
Deletion mapping of H-Y antigen to the long arm of the human Y chromosome
M A Cantrell, J S Bogan, E Simpson, et al.
American Journal of Medical Genetics
|
June 28, 2001
Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3
D N Schweitzer, J M Graham, R S Lachman, et al.
European Journal of Clinical Investigation
|
March 19, 2003
Effects of insulin lispro and chronic vitamin C therapy on postprandial lipaemia, oxidative stress and endothelial function in patients with type 2 diabetes mellitus
M Evans, R A Anderson, J C Smith, et al.
Neurology
|
December 15, 2004
Diffusion tensor imaging for the assessment of upper motor neuron integrity in ALS
J M Graham, N Papadakis, J Evans, et al.
American Journal of Medical Genetics
|
October 2, 1996
Report from the workshop on Pallister-Hall syndrome and related phenotypes
L G Biesecker, M Abbott, J Allen, et al.
Journal of Medical Genetics
|
January 15, 2003
P63 mutations are not a major cause of non-syndromic split hand/foot malformation
X J de Mollerat, D B Everman, C T Morgan, et al.
American Journal of Human Genetics
|
March 1, 1996
FGFR2 exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: evidence for missense changes, insertions, and a deletion due to alternative RNA splicing
G A Meyers, D Day, R Goldberg, et al.
Page
of 36