A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3

Nature Genetics

Volumn 6, Issue 2, 1994, Pages 205-209

  Shovlin, Claire L ^a,b,c   Hughes, J M B ^b   Tuddenham, E G D ^d   Temperley, I ^e   Perembelon, Y F N ^a   Scott, J ^a   Seidman, Christine E ^f   Seidman, J G ^c  

^a HAMMERSMITH HOSPITAL   (United Kingdom)

^b IMPERIAL COLLEGE LONDON   (United Kingdom)

^c HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^d MRC Clinical Research Centre   (United Kingdom)

^e TRINITY COLLEGE DUBLIN   (Ireland)

^f HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN TYPE 5;

ARTERIOVENOUS SHUNT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 9Q; CLINICAL FEATURE; GENE EXPRESSION; GENE MAPPING; GENETIC LINKAGE; HUMAN; PRIORITY JOURNAL; RECURRENT DISEASE; RENDU OSLER WEBER DISEASE;

ADULT; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 9; EUROPE; FEMALE; GENETIC MARKERS; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); MALE; PEDIGREE; POLYMORPHISM, GENETIC; REPETITIVE SEQUENCES, NUCLEIC ACID; TELANGIECTASIA, HEREDITARY HEMORRHAGIC;

EID: 0028239861     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng0294-205     Document Type: Article

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