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American Journal of Diseases of Children (1960)
|
May 1, 1982
Fragile X-linked mental retardation. A survey of 65 patients with mental retardation of unknown origin
N J Carpenter, L G Leichtman, B Say
American Journal of Diseases of Children (1960)
|
April 1, 1979
Genital malformations in a child with VATER association
B Say, N J Carpenter, E I Smith
Journal of Medical Genetics
|
December 1, 1980
Agenesis of the lung associated with a chromosome abnormality (46,XX,2p+)
B Say, N J Carpenter, G Giacoia, et al.
The Journal of the Oklahoma State Medical Association
|
February 1, 1985
Turner syndrome: clinical investigations and review
D P Wilson, N J Carpenter, J H Holcombe
Annales De Genetique
|
January 1, 1997
Clinical applications of primed in situ labelling (PRINS) rapid identification of a marker chromosome in a fetus
G V Velagaleti, N J Carpenter, A T Tharapel
American Journal of Medical Genetics
|
February 1, 1991
Martin-Bell syndrome segregating in a large kindred with normal transmitting males: clinical, cytogenetic, and linkage study
V P Johnson, N J Carpenter, P A Skorey
American Journal of Medical Genetics
|
February 1, 1991
Linkage relationships between DXS105, DXS98, and other polymorphic DNA markers flanking the fragile X locus
N J Carpenter, S N Thibodeau, W T Brown
American Journal of Medical Genetics
|
December 1, 1991
Pelizaeus-Merzbacher disease: clinical and DNA-linkage study of an extended family
V P Johnson, N J Carpenter, K A Kelts
Journal of Medical Genetics
|
June 1, 1981
An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome?
N J Carpenter, L G Leichtman, S Stamper, et al.
American Journal of Medical Genetics
|
July 9, 1999
X-linked mental retardation syndrome with characteristic "coarse" facial appearance, brachydactyly, and short stature maps to proximal Xq
N J Carpenter, Y Qu, M Curtis, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 59) with videos related to
Sort By:
Page
of 6
American Journal of Diseases of Children (1960)
|
May 1, 1982
Fragile X-linked mental retardation. A survey of 65 patients with mental retardation of unknown origin
N J Carpenter, L G Leichtman, B Say
American Journal of Diseases of Children (1960)
|
April 1, 1979
Genital malformations in a child with VATER association
B Say, N J Carpenter, E I Smith
Journal of Medical Genetics
|
December 1, 1980
Agenesis of the lung associated with a chromosome abnormality (46,XX,2p+)
B Say, N J Carpenter, G Giacoia, et al.
The Journal of the Oklahoma State Medical Association
|
February 1, 1985
Turner syndrome: clinical investigations and review
D P Wilson, N J Carpenter, J H Holcombe
Annales De Genetique
|
January 1, 1997
Clinical applications of primed in situ labelling (PRINS) rapid identification of a marker chromosome in a fetus
G V Velagaleti, N J Carpenter, A T Tharapel
American Journal of Medical Genetics
|
February 1, 1991
Martin-Bell syndrome segregating in a large kindred with normal transmitting males: clinical, cytogenetic, and linkage study
V P Johnson, N J Carpenter, P A Skorey
American Journal of Medical Genetics
|
February 1, 1991
Linkage relationships between DXS105, DXS98, and other polymorphic DNA markers flanking the fragile X locus
N J Carpenter, S N Thibodeau, W T Brown
American Journal of Medical Genetics
|
December 1, 1991
Pelizaeus-Merzbacher disease: clinical and DNA-linkage study of an extended family
V P Johnson, N J Carpenter, K A Kelts
Journal of Medical Genetics
|
June 1, 1981
An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome?
N J Carpenter, L G Leichtman, S Stamper, et al.
American Journal of Medical Genetics
|
July 9, 1999
X-linked mental retardation syndrome with characteristic "coarse" facial appearance, brachydactyly, and short stature maps to proximal Xq
N J Carpenter, Y Qu, M Curtis, et al.
Page
of 6