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N L Rudd

Showing results (1-10 of 42) with videos related to

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L' Infirmiere Canadienne|January 1, 1977
[Dilemma: prenatal diagnosis using amniocentesis]N L Rudd, B M Youson
Clinical Genetics|September 1, 1990
Familial caudal dysgenesis: evidence for a major dominant geneN L Rudd, M L Klimek
American Journal of Medical Genetics|January 1, 1988
A case of ring (9)/del(9p) mosaicism associated with gastroesophageal refluxA K Leung, N L Rudd
Lancet (London, England)|May 29, 1976
Letter: Prenatal diagnosis of hypophosphatasiaD I Hoar, N L Rudd
Human Genetics|January 1, 1983
The association of a lymphoreticular malignancy with an 11q deletion: a coincidence or a cancer susceptibility?N L Rudd, I E Teshima
The Canadian Nurse|August 1, 1976
DilemmaN L Rudd, B M Youson
Teratology|October 1, 1976
Craniosynostosis. I. Sagittal synostosis: its genetics and associated clinical findings in 214 patients who lacked involvement of the coronal suture(s)A G Hunter, N L Rudd
Birth Defects Original Article Series|January 1, 1977
The natural history of aminopterin-induced embryopathyN J Howard, N L Rudd
Journal of Medical Genetics|March 1, 1971
Gene deletion and duplication effects on phenotype and gamma globulin levelsN L Rudd, P H Lamarche
Teratology|June 1, 1977
Craniosynostosis. II. Coronal synostosis: its familial characteristics and associated clinical findings in 109 patients lacking bilateral polysyndactyly or syndactylyA G Hunter, N L Rudd
Pageof 5

Showing results (1-10 of 42) with videos related to

Sort By:
Pageof 5
L' Infirmiere Canadienne|January 1, 1977
[Dilemma: prenatal diagnosis using amniocentesis]N L Rudd, B M Youson
Clinical Genetics|September 1, 1990
Familial caudal dysgenesis: evidence for a major dominant geneN L Rudd, M L Klimek
American Journal of Medical Genetics|January 1, 1988
A case of ring (9)/del(9p) mosaicism associated with gastroesophageal refluxA K Leung, N L Rudd
Lancet (London, England)|May 29, 1976
Letter: Prenatal diagnosis of hypophosphatasiaD I Hoar, N L Rudd
Human Genetics|January 1, 1983
The association of a lymphoreticular malignancy with an 11q deletion: a coincidence or a cancer susceptibility?N L Rudd, I E Teshima
The Canadian Nurse|August 1, 1976
DilemmaN L Rudd, B M Youson
Teratology|October 1, 1976
Craniosynostosis. I. Sagittal synostosis: its genetics and associated clinical findings in 214 patients who lacked involvement of the coronal suture(s)A G Hunter, N L Rudd
Birth Defects Original Article Series|January 1, 1977
The natural history of aminopterin-induced embryopathyN J Howard, N L Rudd
Journal of Medical Genetics|March 1, 1971
Gene deletion and duplication effects on phenotype and gamma globulin levelsN L Rudd, P H Lamarche
Teratology|June 1, 1977
Craniosynostosis. II. Coronal synostosis: its familial characteristics and associated clinical findings in 109 patients lacking bilateral polysyndactyly or syndactylyA G Hunter, N L Rudd
Pageof 5