Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22

Human Genetics

Volumn 106, Issue 3, 2000, Pages 351-354

  Afzal, A R ^a   Rajab, A ^d   Fenske, C ^a   Crosby, A ^a   Lahiri, N ^a   Ternes Pereira, E ^b   Murday, V A ^a   Houlston, R ^c   Patton, M A ^a   Jeffery, S ^a  

^a ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

^b FEDERAL UNIVERSITY OF SANTA CATARINA   (Brazil)

^c INSTITUTE OF CANCER RESEARCH   (United Kingdom)

^d MINISTRY OF HEALTH   (Oman)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOME 9Q; CLINICAL ARTICLE; CONSANGUINITY; CONTROLLED STUDY; DWARFISM; GENE LOCUS; GENE MAPPING; GENETIC HETEROGENEITY; GENETIC LINKAGE; HUMAN; OMAN; PRIORITY JOURNAL; RIB MALFORMATION; ROBINOW SYNDROME; VERTEBRA MALFORMATION;

BONE AND BONES; BRAZIL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 9; CONSANGUINITY; DWARFISM; GENES, RECESSIVE; GREAT BRITAIN; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); LOD SCORE; MICROSATELLITE REPEATS; OMAN;

EID: 19244377450     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390051049     Document Type: Article

References (10)

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