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A L Shanske

Showing results (1-10 of 19) with videos related to

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Archives of Pediatrics & Adolescent Medicine|November 29, 2001
The other human genomeA L Shanske, S Shanske, S DiMauro
British Journal of Haematology|December 1, 1996
A myeloproliferative disorder with eosinophilia associated with a unique translocation (3;5)A L Shanske, A Kalman, H Grunwald
The Journal of Clinical Pediatric Dentistry|January 1, 1993
Natal molars in Pfeiffer syndrome type 3: a case reportM P Alvarez, P V Crespi, A L Shanske
Birth Defects Original Article Series|January 1, 1982
A possible lethal variant of metatropic dwarfismA L Shanske, M Baden, M Fernando, et al.
American Journal of Medical Genetics|May 2, 1997
The Marshall syndrome: report of a new family and review of the literatureA L Shanske, A Bogdanow, R J Shprintzen, et al.
American Journal of Medical Genetics. Part A|July 21, 2004
Mutations in IRF6 do not cause Bartsocas-Papas syndrome in a family with two affected sibsA L Shanske, S A Hoper, K Krahn, et al.
Leukemia Research|July 29, 1998
Philadelphia-negative chronic myelogenous leukemia in a patient with a unique complex translocation: 46,XY,t(9;12;15)(q34;12;q21)A L Shanske, H Grunwald, P Cook, et al.
American Journal of Medical Genetics. Part A|September 16, 2004
Detection of an interstitial deletion of 2q21-22 by high resolution comparative genomic hybridization in a child with multiple congenital anomalies and an apparent balanced translocationA L Shanske, L Edelmann, N B Kardon, et al.
Neuropediatrics|August 1, 1991
Duchenne muscular dystrophy in a girl identified by dystrophin deficiencyJ Maytal, A L Shanske, J E Fox, et al.
American Journal of Medical Genetics. Part A|November 26, 2010
Delineation of the breakpoints of pure duplication 3q due to a de novo duplication event using SOMAA L Shanske, J Leonard, O Nahum, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Archives of Pediatrics & Adolescent Medicine|November 29, 2001
The other human genomeA L Shanske, S Shanske, S DiMauro
British Journal of Haematology|December 1, 1996
A myeloproliferative disorder with eosinophilia associated with a unique translocation (3;5)A L Shanske, A Kalman, H Grunwald
The Journal of Clinical Pediatric Dentistry|January 1, 1993
Natal molars in Pfeiffer syndrome type 3: a case reportM P Alvarez, P V Crespi, A L Shanske
Birth Defects Original Article Series|January 1, 1982
A possible lethal variant of metatropic dwarfismA L Shanske, M Baden, M Fernando, et al.
American Journal of Medical Genetics|May 2, 1997
The Marshall syndrome: report of a new family and review of the literatureA L Shanske, A Bogdanow, R J Shprintzen, et al.
American Journal of Medical Genetics. Part A|July 21, 2004
Mutations in IRF6 do not cause Bartsocas-Papas syndrome in a family with two affected sibsA L Shanske, S A Hoper, K Krahn, et al.
Leukemia Research|July 29, 1998
Philadelphia-negative chronic myelogenous leukemia in a patient with a unique complex translocation: 46,XY,t(9;12;15)(q34;12;q21)A L Shanske, H Grunwald, P Cook, et al.
American Journal of Medical Genetics. Part A|September 16, 2004
Detection of an interstitial deletion of 2q21-22 by high resolution comparative genomic hybridization in a child with multiple congenital anomalies and an apparent balanced translocationA L Shanske, L Edelmann, N B Kardon, et al.
Neuropediatrics|August 1, 1991
Duchenne muscular dystrophy in a girl identified by dystrophin deficiencyJ Maytal, A L Shanske, J E Fox, et al.
American Journal of Medical Genetics. Part A|November 26, 2010
Delineation of the breakpoints of pure duplication 3q due to a de novo duplication event using SOMAA L Shanske, J Leonard, O Nahum, et al.
Pageof 2