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Journal of Medical Genetics
|
December 1, 1977
A 'new' syndrome of mental retardation with characteristic facies and brachyphalangy
A G Hunter, P J McAlpine, N L Rudd, et al.
The Journal of Pediatrics
|
September 1, 1979
Arthrogryposis multiplex congenita--prenatal assessment with diagnostic ultrasound and fetoscopy
M Miskin, R Rothberg, N L Rudd, et al.
Genome
|
April 1, 1989
Genotype and the cryopreservation process affect the levels of aneuploidy and chromosome breakage in cultured human fibroblasts
N L Rudd, D I Hoar, S E Williams, et al.
Birth Defects Original Article Series
|
January 1, 1978
Autosomal imbalance with a near-normal phenotype: the small effect of trisomy for the short arm of chromosome 18
R J Gardner, N L Rudd, L J Stevens, et al.
American Journal of Obstetrics and Gynecology
|
March 1, 1978
Prenatal ultrasonic diagnosis of occipital encephalocele
M Miskin, N L Rudd, M R Dische, et al.
Canadian Journal of Genetics and Cytology. Journal Canadien De Genetique Et De Cytologie
|
October 1, 1984
Factors distinguishing couples at risk for nondisjunction
N L Rudd, D I Hoar, R H Martin, et al.
The New England Journal of Medicine
|
July 15, 1976
Prenatal diagnosis of hypophosphatasia
N L Rudd, M Miskin, D I Hoar, et al.
American Journal of Medical Genetics
|
November 1, 1990
Thymic-renal-anal-lung dysplasia in sibs: a new autosomal recessive error of early morphogenesis
N L Rudd, C Curry, K T Chen, et al.
Human Genetics
|
January 1, 1983
A dominantly inherited cytogenetic anomaly: a possible cell division mutant
N L Rudd, I E Teshima, R H Martin, et al.
Human Genetics
|
February 1, 1988
The use of DNA probes to establish parental origin in Down syndrome
N L Rudd, L S Dimnik, C Greentree, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 42) with videos related to
Sort By:
Page
of 5
Journal of Medical Genetics
|
December 1, 1977
A 'new' syndrome of mental retardation with characteristic facies and brachyphalangy
A G Hunter, P J McAlpine, N L Rudd, et al.
The Journal of Pediatrics
|
September 1, 1979
Arthrogryposis multiplex congenita--prenatal assessment with diagnostic ultrasound and fetoscopy
M Miskin, R Rothberg, N L Rudd, et al.
Genome
|
April 1, 1989
Genotype and the cryopreservation process affect the levels of aneuploidy and chromosome breakage in cultured human fibroblasts
N L Rudd, D I Hoar, S E Williams, et al.
Birth Defects Original Article Series
|
January 1, 1978
Autosomal imbalance with a near-normal phenotype: the small effect of trisomy for the short arm of chromosome 18
R J Gardner, N L Rudd, L J Stevens, et al.
American Journal of Obstetrics and Gynecology
|
March 1, 1978
Prenatal ultrasonic diagnosis of occipital encephalocele
M Miskin, N L Rudd, M R Dische, et al.
Canadian Journal of Genetics and Cytology. Journal Canadien De Genetique Et De Cytologie
|
October 1, 1984
Factors distinguishing couples at risk for nondisjunction
N L Rudd, D I Hoar, R H Martin, et al.
The New England Journal of Medicine
|
July 15, 1976
Prenatal diagnosis of hypophosphatasia
N L Rudd, M Miskin, D I Hoar, et al.
American Journal of Medical Genetics
|
November 1, 1990
Thymic-renal-anal-lung dysplasia in sibs: a new autosomal recessive error of early morphogenesis
N L Rudd, C Curry, K T Chen, et al.
Human Genetics
|
January 1, 1983
A dominantly inherited cytogenetic anomaly: a possible cell division mutant
N L Rudd, I E Teshima, R H Martin, et al.
Human Genetics
|
February 1, 1988
The use of DNA probes to establish parental origin in Down syndrome
N L Rudd, L S Dimnik, C Greentree, et al.
Page
of 5