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Journal of Medical Education
|
September 1, 1978
Genetic associate training program
K W Dumars
The Hastings Center Report
|
December 1, 1979
The two faces of big brother
K W Dumars
Pediatrics
|
June 1, 1971
Parental drug usage: effect upon chromosomes of progeny
K W Dumars
JAMA
|
March 28, 1977
Minimizing the risk of amniocentesis for prenatal diagnosis
A I Goldstein, K W Dumars
Pediatrics
|
December 1, 1973
Cutis aplasia and cerebral malformation
G W Fowler, K W Dumars
American Journal of Medical Genetics
|
January 1, 1981
Duplication of distal 11q and 22p occurrence in two unrelated families
T M Najafzadeh, K W Dumars
Birth Defects Original Article Series
|
January 1, 1976
E trisomy phenotype associated with small metacentric chromosome and a familial Y-22 translocation
K W Dumars, G Fialko, E Larson
American Journal of Diseases of Children (1960)
|
November 1, 1976
Prenatal diagnosis of XYY karyotype
K W Dumars, G Fialko, J Willis
Birth Defects Original Article Series
|
January 1, 1982
Etiologic heterogeneity in hydranencephaly
T M Najafzadeh, L Reinisch, K W Dumars
Birth Defects Original Article Series
|
January 1, 1975
X-autosome translocation with a 47,XXXY qs,t(9p-;Xq+) karyotype
K W Dumars, P Reed, H J Lawce
Page
of 3
Search research articles
Search
Showing results (1-10 of 29) with videos related to
Sort By:
Page
of 3
Journal of Medical Education
|
September 1, 1978
Genetic associate training program
K W Dumars
The Hastings Center Report
|
December 1, 1979
The two faces of big brother
K W Dumars
Pediatrics
|
June 1, 1971
Parental drug usage: effect upon chromosomes of progeny
K W Dumars
JAMA
|
March 28, 1977
Minimizing the risk of amniocentesis for prenatal diagnosis
A I Goldstein, K W Dumars
Pediatrics
|
December 1, 1973
Cutis aplasia and cerebral malformation
G W Fowler, K W Dumars
American Journal of Medical Genetics
|
January 1, 1981
Duplication of distal 11q and 22p occurrence in two unrelated families
T M Najafzadeh, K W Dumars
Birth Defects Original Article Series
|
January 1, 1976
E trisomy phenotype associated with small metacentric chromosome and a familial Y-22 translocation
K W Dumars, G Fialko, E Larson
American Journal of Diseases of Children (1960)
|
November 1, 1976
Prenatal diagnosis of XYY karyotype
K W Dumars, G Fialko, J Willis
Birth Defects Original Article Series
|
January 1, 1982
Etiologic heterogeneity in hydranencephaly
T M Najafzadeh, L Reinisch, K W Dumars
Birth Defects Original Article Series
|
January 1, 1975
X-autosome translocation with a 47,XXXY qs,t(9p-;Xq+) karyotype
K W Dumars, P Reed, H J Lawce
Page
of 3