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H Shalev

Showing results (31-40 of 44) with videos related to

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Prenatal Diagnosis|March 22, 2001
Prenatal diagnosis of malignant osteopetrosis in Bedouin families by linkage analysisH Shalev, A Mishori-Dery, J Kapelushnik, et al.
Pediatric Nephrology (Berlin, Germany)|November 12, 1998
Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor HM Ohali, H Shalev, M Schlesinger, et al.
Human Molecular Genetics|August 13, 1998
Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutationC Heaney, H Shalev, K Elbedour, et al.
European Journal of Haematology|June 19, 2002
Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in young adultsH Shalev, Y Kapleushnik, L Haeskelzon, et al.
American Journal of Human Genetics|December 1, 1999
Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndromeL Ying, Y Katz, M Schlesinger, et al.
Neurology|January 14, 2004
Infantile bilateral striatal necrosis maps to chromosome 19qL Basel-Vanagaite, R Straussberg, H Ovadia, et al.
British Journal of Haematology|September 21, 2001
Glycoconjugate abnormalities in patients with congenital dyserythropoietic anaemia type I, II and IIIE Zdebska, E Gołaszewska, J Fabijańska-Mitek, et al.
American Journal of Human Genetics|May 23, 1998
Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3H Tamary, L Shalmon, H Shalev, et al.
BMC Psychiatry|June 13, 2023
Neuro-psychiatric symptoms in directly and indirectly blast exposed civilian survivors of urban missile attacksR Saar-Ashkenazy, S Naparstek, Y Dizitzer, et al.
American Journal of Human Genetics|April 16, 1998
Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1pT M Brennan, D Landau, H Shalev, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Prenatal Diagnosis|March 22, 2001
Prenatal diagnosis of malignant osteopetrosis in Bedouin families by linkage analysisH Shalev, A Mishori-Dery, J Kapelushnik, et al.
Pediatric Nephrology (Berlin, Germany)|November 12, 1998
Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor HM Ohali, H Shalev, M Schlesinger, et al.
Human Molecular Genetics|August 13, 1998
Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutationC Heaney, H Shalev, K Elbedour, et al.
European Journal of Haematology|June 19, 2002
Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in young adultsH Shalev, Y Kapleushnik, L Haeskelzon, et al.
American Journal of Human Genetics|December 1, 1999
Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndromeL Ying, Y Katz, M Schlesinger, et al.
Neurology|January 14, 2004
Infantile bilateral striatal necrosis maps to chromosome 19qL Basel-Vanagaite, R Straussberg, H Ovadia, et al.
British Journal of Haematology|September 21, 2001
Glycoconjugate abnormalities in patients with congenital dyserythropoietic anaemia type I, II and IIIE Zdebska, E Gołaszewska, J Fabijańska-Mitek, et al.
American Journal of Human Genetics|May 23, 1998
Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3H Tamary, L Shalmon, H Shalev, et al.
BMC Psychiatry|June 13, 2023
Neuro-psychiatric symptoms in directly and indirectly blast exposed civilian survivors of urban missile attacksR Saar-Ashkenazy, S Naparstek, Y Dizitzer, et al.
American Journal of Human Genetics|April 16, 1998
Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1pT M Brennan, D Landau, H Shalev, et al.
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