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R L Ladda

Showing results (21-30 of 67) with videos related to

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Journal of Medical Genetics|December 1, 1981
Hereditary multiple exostoses: report of a kindredS L Gordon, J R Buchanan, R L Ladda
Blood|April 1, 1977
Carriers with excessively low factor VIII procoagulant activity (VIII AHF): a study of two unrelated families with mild hemophilia AM E Eyster, R L Ladda, H S Bowman
Journal of Medical Genetics|January 1, 1994
Familial leuconychia, knuckle pads, hearing loss, and palmoplantar hyperkeratosis: an additional family with Bart-Pumphrey syndromeJ C Ramer, D B Vasily, R L Ladda
American Journal of Medical Genetics|September 1, 1988
Dandy-Walker malformation in Ellis-van Creveld syndromeK M Zangwill, D K Boal, R L Ladda
American Journal of Diseases of Children (1960)|January 1, 1978
Hypothyroidism in an infant with Down's syndromeS L King, R L Ladda, H E Kulin
Acta Paediatrica Scandinavica|November 1, 1977
Monozygotic twins concordant for tracheo-esophageal fistula and discordant for the VATER associationS L King, R L Ladda, S J Shochat
Clinical Genetics|June 1, 1991
Malformations in a child with dup (7pter-p15.1) and del (7q36-qter) as a result of familial pericentric inversionJ C Ramer, P N Mowrey, R L Ladda
American Journal of Diseases of Children (1960)|July 1, 1988
Multiple pterygium syndrome. An overviewJ C Ramer, R L Ladda, W W Demuth
Mechanisms of Ageing and Development|March 1, 1986
Receptor for epidermal growth factor retains normal structure and function in aging cellsC C Chua, D E Geiman, R L Ladda
American Journal of Medical Genetics|February 1, 1993
Marden-Walker phenotype: spectrum of variability in three infantsJ C Ramer, C A Frankel, R L Ladda
Pageof 7

Showing results (21-30 of 67) with videos related to

Sort By:
Pageof 7
Journal of Medical Genetics|December 1, 1981
Hereditary multiple exostoses: report of a kindredS L Gordon, J R Buchanan, R L Ladda
Blood|April 1, 1977
Carriers with excessively low factor VIII procoagulant activity (VIII AHF): a study of two unrelated families with mild hemophilia AM E Eyster, R L Ladda, H S Bowman
Journal of Medical Genetics|January 1, 1994
Familial leuconychia, knuckle pads, hearing loss, and palmoplantar hyperkeratosis: an additional family with Bart-Pumphrey syndromeJ C Ramer, D B Vasily, R L Ladda
American Journal of Medical Genetics|September 1, 1988
Dandy-Walker malformation in Ellis-van Creveld syndromeK M Zangwill, D K Boal, R L Ladda
American Journal of Diseases of Children (1960)|January 1, 1978
Hypothyroidism in an infant with Down's syndromeS L King, R L Ladda, H E Kulin
Acta Paediatrica Scandinavica|November 1, 1977
Monozygotic twins concordant for tracheo-esophageal fistula and discordant for the VATER associationS L King, R L Ladda, S J Shochat
Clinical Genetics|June 1, 1991
Malformations in a child with dup (7pter-p15.1) and del (7q36-qter) as a result of familial pericentric inversionJ C Ramer, P N Mowrey, R L Ladda
American Journal of Diseases of Children (1960)|July 1, 1988
Multiple pterygium syndrome. An overviewJ C Ramer, R L Ladda, W W Demuth
Mechanisms of Ageing and Development|March 1, 1986
Receptor for epidermal growth factor retains normal structure and function in aging cellsC C Chua, D E Geiman, R L Ladda
American Journal of Medical Genetics|February 1, 1993
Marden-Walker phenotype: spectrum of variability in three infantsJ C Ramer, C A Frankel, R L Ladda
Pageof 7