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R L Ladda

Showing results (51-60 of 67) with videos related to

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American Journal of Medical Genetics|September 15, 1993
Congenital contractures, ectodermal dysplasia, cleft lip/palate, and developmental impairment: a distinct syndromeR L Ladda, J Zonana, J C Ramer, et al.
American Journal of Obstetrics and Gynecology|November 1, 1979
Establishment and characterization of a new endometrial cancer cell line (SCRC-1)J Gorodecki, R Mortel, R L Ladda, et al.
Archives of Pathology & Laboratory Medicine|July 1, 1985
Neuropathology of oral-facial-digital syndromesJ Towfighi, C M Berlin, R L Ladda, et al.
American Journal of Medical Genetics|September 1, 1990
Neurologic manifestations in 18q- syndromeG Miller, P N Mowrey, K D Hopper, et al.
American Journal of Obstetrics and Gynecology|May 15, 1982
Prenatal diagnosis of Duchenne muscular dystrophy: failure of amniotic fluid and maternal serum N tau-methylhistidine analyses to detect affected fetusesS J Wassner, J B Li, R L Ladda, et al.
American Journal of Medical Genetics|September 15, 1992
Cutaneous scar at anterior hair line in mother and child with associated frontal bone defect in childJ P Stratis, J C Ramer, E K Manders, et al.
Obstetrics and Gynecology|April 1, 1980
Chromosomal abnormalities associated with infertilityJ M Sulewski, T P Dang, K A Ferguson, et al.
Human Molecular Genetics|June 1, 1994
A new missense mutation, Arg719Gln, in the beta-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathyM W Consevage, G C Salada, B G Baylen, et al.
American Journal of Medical Genetics|November 1, 1990
Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: review of brain, cardiac, and limb malformationsJ C Ramer, P N Mowrey, D B Robins, et al.
American Journal of Medical Genetics|December 18, 1995
Absence of linkage of apparently single gene mediated ADHD with the human syntenic region of the mouse mutant ColobomaE J Hess, P K Rogan, M Domoto, et al.
Pageof 7

Showing results (51-60 of 67) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics|September 15, 1993
Congenital contractures, ectodermal dysplasia, cleft lip/palate, and developmental impairment: a distinct syndromeR L Ladda, J Zonana, J C Ramer, et al.
American Journal of Obstetrics and Gynecology|November 1, 1979
Establishment and characterization of a new endometrial cancer cell line (SCRC-1)J Gorodecki, R Mortel, R L Ladda, et al.
Archives of Pathology & Laboratory Medicine|July 1, 1985
Neuropathology of oral-facial-digital syndromesJ Towfighi, C M Berlin, R L Ladda, et al.
American Journal of Medical Genetics|September 1, 1990
Neurologic manifestations in 18q- syndromeG Miller, P N Mowrey, K D Hopper, et al.
American Journal of Obstetrics and Gynecology|May 15, 1982
Prenatal diagnosis of Duchenne muscular dystrophy: failure of amniotic fluid and maternal serum N tau-methylhistidine analyses to detect affected fetusesS J Wassner, J B Li, R L Ladda, et al.
American Journal of Medical Genetics|September 15, 1992
Cutaneous scar at anterior hair line in mother and child with associated frontal bone defect in childJ P Stratis, J C Ramer, E K Manders, et al.
Obstetrics and Gynecology|April 1, 1980
Chromosomal abnormalities associated with infertilityJ M Sulewski, T P Dang, K A Ferguson, et al.
Human Molecular Genetics|June 1, 1994
A new missense mutation, Arg719Gln, in the beta-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathyM W Consevage, G C Salada, B G Baylen, et al.
American Journal of Medical Genetics|November 1, 1990
Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: review of brain, cardiac, and limb malformationsJ C Ramer, P N Mowrey, D B Robins, et al.
American Journal of Medical Genetics|December 18, 1995
Absence of linkage of apparently single gene mediated ADHD with the human syntenic region of the mouse mutant ColobomaE J Hess, P K Rogan, M Domoto, et al.
Pageof 7