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Journal of Medical Genetics
|
June 1, 1990
The Baller-Gerold syndrome: phenotypic and cytogenetic overlap with Roberts syndrome
S M Huson, C S Rodgers, C M Hall, et al.
Annals of the New York Academy of Sciences
|
January 1, 1988
Genetic counselling in perinatally lethal and severe progressively deforming osteogenesis imperfecta
E M Thompson, I D Young, C M Hall, et al.
Clinical Genetics
|
December 1, 1989
Phenotypical features of an unique Irish family with severe autosomal recessive Osteogenesis imperfecta
E M Thompson, I D Young, C M Hall, et al.
Journal of Medicinal Chemistry
|
September 1, 1978
Structure-activity correlations for a series of antiallergy agents. Oxanilic, quinaldic, and benzopyran-2-carboxylic acids
B V Cheney, J B Wright, C M Hall, et al.
Epilepsia
|
July 1, 1989
Identification of a median thalamic system regulating seizures and arousal
J W Miller, C M Hall, K D Holland, et al.
The British Journal of Radiology
|
October 1, 1980
Acromesomelic dwarfism
C M Hall, D J Stoker, D C Robinson, et al.
Clinical Dysmorphology
|
July 1, 1996
Nance-Sweeney chondrodysplasia--a further case?
E M Rosser, C M Hall, J Harper, et al.
Clinical Dysmorphology
|
May 13, 1999
A new syndrome of spondyloepimetaphyseal dysplasia, eczema and hypogammaglobulinaemia
S F Slaney, C M Hall, D J Atherton, et al.
Journal of Medical Genetics
|
July 1, 1987
Osteogenesis imperfecta type IIA: evidence for dominant inheritance
I D Young, E M Thompson, C M Hall, et al.
Journal of Medical Genetics
|
July 1, 1987
Recurrence risks and prognosis in severe sporadic osteogenesis imperfecta
E M Thompson, I D Young, C M Hall, et al.
Page
of 19
Search research articles
Search
Showing results (111-120 of 188) with videos related to
Sort By:
Page
of 19
Journal of Medical Genetics
|
June 1, 1990
The Baller-Gerold syndrome: phenotypic and cytogenetic overlap with Roberts syndrome
S M Huson, C S Rodgers, C M Hall, et al.
Annals of the New York Academy of Sciences
|
January 1, 1988
Genetic counselling in perinatally lethal and severe progressively deforming osteogenesis imperfecta
E M Thompson, I D Young, C M Hall, et al.
Clinical Genetics
|
December 1, 1989
Phenotypical features of an unique Irish family with severe autosomal recessive Osteogenesis imperfecta
E M Thompson, I D Young, C M Hall, et al.
Journal of Medicinal Chemistry
|
September 1, 1978
Structure-activity correlations for a series of antiallergy agents. Oxanilic, quinaldic, and benzopyran-2-carboxylic acids
B V Cheney, J B Wright, C M Hall, et al.
Epilepsia
|
July 1, 1989
Identification of a median thalamic system regulating seizures and arousal
J W Miller, C M Hall, K D Holland, et al.
The British Journal of Radiology
|
October 1, 1980
Acromesomelic dwarfism
C M Hall, D J Stoker, D C Robinson, et al.
Clinical Dysmorphology
|
July 1, 1996
Nance-Sweeney chondrodysplasia--a further case?
E M Rosser, C M Hall, J Harper, et al.
Clinical Dysmorphology
|
May 13, 1999
A new syndrome of spondyloepimetaphyseal dysplasia, eczema and hypogammaglobulinaemia
S F Slaney, C M Hall, D J Atherton, et al.
Journal of Medical Genetics
|
July 1, 1987
Osteogenesis imperfecta type IIA: evidence for dominant inheritance
I D Young, E M Thompson, C M Hall, et al.
Journal of Medical Genetics
|
July 1, 1987
Recurrence risks and prognosis in severe sporadic osteogenesis imperfecta
E M Thompson, I D Young, C M Hall, et al.
Page
of 19