Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutation

Human Molecular Genetics

Volumn 7, Issue 9, 1998, Pages 1407-1410

  Heaney, Conor ^a   Shalev, Hana ^c   Elbedour, Khalil ^c   Carmi, Rivka ^c   Staack, Jeffrey B ^a   Sheffield, Val C ^a,b   Beier, David R ^c,d  

^a UNIVERSITY OF IOWA   (United States)

^b UNIVERSITY OF IOWA   (United States)

^c BEN GURION UNIVERSITY OF THE NEGEV   (Israel)

^d BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA;

ALBERS SCHOENBERG DISEASE; ANEMIA; ARAB; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BLINDNESS; BONE DENSITY; BONE MARROW TRANSPLANTATION; CHILD; CHROMOSOME 11Q; CHROMOSOME 19; CLINICAL ARTICLE; CONSANGUINITY; FEMALE; GENE MAPPING; GENETIC RECOMBINATION; HEARING IMPAIRMENT; HEPATOSPLENOMEGALY; HUMAN; INFANT; LETHALITY; MALE; MOUSE; NONHUMAN; OSTEOCLAST; OSTEOLYSIS; OSTEOSCLEROSIS; PHENOTYPE; PRIORITY JOURNAL; SYNTENY;

ANIMALS; CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 11; CONSANGUINITY; DISEASE MODELS, ANIMAL; FEMALE; GENES, RECESSIVE; HUMANS; INFANT; LOD SCORE; MALE; MICE; MICROSATELLITE REPEATS; MUTATION; OSTEOPETROSIS; OSTEOSCLEROSIS; PEDIGREE;

MURINAE;

EID: 0031656797     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/7.9.1407     Document Type: Article

References (28)

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