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R B Lowry

Showing results (111-120 of 123) with videos related to

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American Journal of Medical Genetics. Part A|November 19, 2009
Father-to-son transmission of an X-linked gene: a case of paternal sex chromosome heterodisomyR A Ferrier, R B Lowry, E G Lemire, et al.
Birth Defects Original Article Series|January 1, 1975
Familial true hermaphroditismR B Lowry, L H Honore, W J Arnold, et al.
La Presse Medicale|May 22, 1971
[The campomelic syndrome]P Maroteaux, J Spranger, J M Opitz, et al.
Ophthalmic Paediatrics and Genetics|June 1, 1987
Autosomal recessive juvenile cataract in HutteritesW G Pearce, J A Mackay, T M Holmes, et al.
American Journal of Medical Genetics|January 1, 1979
The Bowen-Conradi syndrome -- a highly lethal autosomal recessive syndrome of microcephaly, micrognathia, low birth weight, and joint deformitiesA G Hunter, S J Woerner, L D Montalvo-Hicks, et al.
The Journal of Pediatrics|January 1, 1982
Errors of morphogenesis: concepts and terms. Recommendations of an international working groupJ Spranger, K Benirschke, J G Hall, et al.
Journal of Medical Genetics|May 16, 2002
Alport syndrome and mental retardation: clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR)I Meloni, F Vitelli, L Pucci, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 1, 1994
Autosomal recessive, fatal infantile hypertonic muscular dystrophy among Canadian NativesA G Lacson, S S Seshia, H B Sarnat, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Co-occurrence of Joubert syndrome and Jeune asphyxiating thoracic dystrophyA M Lehman, P Eydoux, D Doherty, et al.
American Journal of Medical Genetics|November 1, 1985
Morquio syndrome (MPS IVA) and hypophosphatasia in a Hutterite kindredR B Lowry, F F Snyder, R L Wesenberg, et al.
Pageof 13

Showing results (111-120 of 123) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics. Part A|November 19, 2009
Father-to-son transmission of an X-linked gene: a case of paternal sex chromosome heterodisomyR A Ferrier, R B Lowry, E G Lemire, et al.
Birth Defects Original Article Series|January 1, 1975
Familial true hermaphroditismR B Lowry, L H Honore, W J Arnold, et al.
La Presse Medicale|May 22, 1971
[The campomelic syndrome]P Maroteaux, J Spranger, J M Opitz, et al.
Ophthalmic Paediatrics and Genetics|June 1, 1987
Autosomal recessive juvenile cataract in HutteritesW G Pearce, J A Mackay, T M Holmes, et al.
American Journal of Medical Genetics|January 1, 1979
The Bowen-Conradi syndrome -- a highly lethal autosomal recessive syndrome of microcephaly, micrognathia, low birth weight, and joint deformitiesA G Hunter, S J Woerner, L D Montalvo-Hicks, et al.
The Journal of Pediatrics|January 1, 1982
Errors of morphogenesis: concepts and terms. Recommendations of an international working groupJ Spranger, K Benirschke, J G Hall, et al.
Journal of Medical Genetics|May 16, 2002
Alport syndrome and mental retardation: clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR)I Meloni, F Vitelli, L Pucci, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 1, 1994
Autosomal recessive, fatal infantile hypertonic muscular dystrophy among Canadian NativesA G Lacson, S S Seshia, H B Sarnat, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Co-occurrence of Joubert syndrome and Jeune asphyxiating thoracic dystrophyA M Lehman, P Eydoux, D Doherty, et al.
American Journal of Medical Genetics|November 1, 1985
Morquio syndrome (MPS IVA) and hypophosphatasia in a Hutterite kindredR B Lowry, F F Snyder, R L Wesenberg, et al.
Pageof 13