Mapping of autosomal dominant osteopetrosis type II (Albers-Schönberg disease) to chromosome 16p13.3

American Journal of Human Genetics

Volumn 69, Issue 3, 2001, Pages 647-654

  Bénichou, Olivier ^a   Cleiren, Erna ^b   Gram, Jeppe ^c   Bollerslev, Jens ^d   De Vernejoul, Marie Christine ^a   Van Hul, Wim ^b  

^a HÔPITAL LARIBOISIÈRE   (France)

^b UNIVERSITY OF ANTWERP   (Belgium)

^c ESBJERG HOSPITAL   (Denmark)

^d OSLO UNIVERSITY HOSPITAL   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

ALBERS SCHOENBERG DISEASE; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; BONE DENSITY; CHROMOSOME 16P; CHROMOSOME 1P; CONTROLLED STUDY; FEMALE; FRACTURE; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENETIC ANALYSIS; GENETIC LINKAGE; GENOME; HUMAN; MAJOR CLINICAL STUDY; MALE; MARKER GENE; OSTEOLYSIS; OSTEOSCLEROSIS; PELVIS; PRIORITY JOURNAL; RISK FACTOR; SCLEROSIS; SKULL BASE; SPINE; VERTEBRA;

EID: 0034894052     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/323132     Document Type: Article

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