Cardiac abnormalities in the Bardet-Biedl syndrome : echocardiographic studies of 22 patientsELBEDOUR, K; ZUCKER, N; ZALZSTEIN, E et al.American journal of medical genetics. 1994, Vol 52, Num 2, pp 164-169, issn 0148-7299Article

Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mappingSHEFFIELD, V. C; CARMI, R; KWITEK-BLACK, A et al.Human molecular genetics (Print). 1994, Vol 3, Num 8, pp 1331-1335, issn 0964-6906Article

Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutationHEANEY, C; SHALEV, H; ELBEDOUR, K et al.Human molecular genetics (Print). 1998, Vol 7, Num 9, pp 1407-1410, issn 0964-6906Article

Familial hypomagnesemia maps to chromosome 9q, not to the X chromosome : genetic linkage mapping and analysis of a balanced translocation breakpointWALDER, R. Y; SHALEV, H; SHEFFIELD, V. C et al.Human molecular genetics (Print). 1997, Vol 6, Num 9, pp 1491-1497, issn 0964-6906Article

An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred bedouin kindredsSCOTT, D. A; CARMI, R; ELBEDOUR, K et al.American journal of human genetics. 1996, Vol 59, Num 2, pp 385-391, issn 0002-9297Article

Phenotypic differences among patients with Bardet-Biedl syndrome linked to three different chromosome lociCARMI, R; ELBEDOUR, K; STONE, E. M et al.American journal of medical genetics. 1995, Vol 59, Num 2, pp 199-203, issn 0148-7299Article