Localization of a gene for autosomal dominant osteopetrosis (Albers- Schonberg disease) to chromosome 1p21

American Journal of Human Genetics

Volumn 61, Issue 2, 1997, Pages 363-369

  Van Hul, Wim ^a   Bollerslev, Jens ^c   Gram, Jeppe ^d   Van Hul, Els ^a   Wuyts, Wim ^a   Benichou, Olivier ^e   Vanhoenacker, Filip ^b   Willems, Patrick J ^a  

^a UNIVERSITY OF ANTWERP   (Belgium)

^b ANTWERP UNIVERSITY HOSPITAL   (Belgium)

^c OSLO UNIVERSITY HOSPITAL   (Norway)

^d ODENSE UNIVERSITY HOSPITAL   (Denmark)

^e HÔPITAL LARIBOISIÈRE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DINUCLEOTIDE; DNA;

ALBERS SCHOENBERG DISEASE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BONE RADIOGRAPHY; CHROMOSOME 1P; CLINICAL ARTICLE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; GENE FREQUENCY; GENE LOCATION; GENE MUTATION; GENETIC LINKAGE; GENOTYPE; HUMAN; MALE; PEDIGREE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0030826426     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/514844     Document Type: Article

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