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R Carmi

Showing results (81-90 of 103) with videos related to

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Pediatric Nephrology (Berlin, Germany)|November 12, 1998
Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor HM Ohali, H Shalev, M Schlesinger, et al.
American Journal of Human Genetics|October 1, 1995
Nonsyndromic autosomal recessive deafness is linked to the DFNB1 locus in a large inbred Bedouin family from IsraelD A Scott, R Carmi, K Elbedour, 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.
Human Molecular Genetics|January 1, 1995
Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15R Carmi, T Rokhlina, A E Kwitek-Black, 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.
American Journal of Medical Genetics|March 4, 2000
Short stature in carriers of recessive mutation causing familial isolated growth hormone deficiencyE Leiberman, D Pesler, R Parvari, et al.
Bone Marrow Transplantation|April 3, 2001
Osteopetrosis: a single centre experience of stem cell tranisplantation and prenatal diagnosisJ Kapelushnik, C Shalev, I Yaniv, et al.
The Israel Medical Association Journal : IMAJ|September 9, 2000
Achondroplasia in diverse Jewish and Arab populations in Israel: clinical and molecular characterizationT C Falik-Zaccai, E Shachak, D Abeliovitch, et al.
Human Molecular Genetics|August 1, 1994
Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mappingV C Sheffield, R Carmi, A Kwitek-Black, 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 11

Showing results (81-90 of 103) with videos related to

Sort By:
Pageof 11
Pediatric Nephrology (Berlin, Germany)|November 12, 1998
Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor HM Ohali, H Shalev, M Schlesinger, et al.
American Journal of Human Genetics|October 1, 1995
Nonsyndromic autosomal recessive deafness is linked to the DFNB1 locus in a large inbred Bedouin family from IsraelD A Scott, R Carmi, K Elbedour, 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.
Human Molecular Genetics|January 1, 1995
Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15R Carmi, T Rokhlina, A E Kwitek-Black, 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.
American Journal of Medical Genetics|March 4, 2000
Short stature in carriers of recessive mutation causing familial isolated growth hormone deficiencyE Leiberman, D Pesler, R Parvari, et al.
Bone Marrow Transplantation|April 3, 2001
Osteopetrosis: a single centre experience of stem cell tranisplantation and prenatal diagnosisJ Kapelushnik, C Shalev, I Yaniv, et al.
The Israel Medical Association Journal : IMAJ|September 9, 2000
Achondroplasia in diverse Jewish and Arab populations in Israel: clinical and molecular characterizationT C Falik-Zaccai, E Shachak, D Abeliovitch, et al.
Human Molecular Genetics|August 1, 1994
Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mappingV C Sheffield, R Carmi, A Kwitek-Black, 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 11