Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21

Proceedings of the National Academy of Sciences of the United States of America

Volumn 92, Issue 14, 1995, Pages 6620-6624

  Günel, Murat ^a,b   Awad, Issam A ^b   Anson, John ^c   Lifton, Richard P ^a,b  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b YALE UNIVERSITY   (United States)

^c UNIVERSITY OF NEW MEXICO HOSPITAL   (United States)

Author keywords

brain; genetics; linkage analysis; vascular malformation

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CEREBROVASCULAR MALFORMATION; CHROMOSOME 7Q; DNA DETERMINATION; GENE LOCATION; GENE MAPPING; GENETIC LINKAGE; HUMAN; MALE; PRIORITY JOURNAL;

BRAIN; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 7; DNA; FEMALE; GENES, DOMINANT; GENETIC MARKERS; GENOME, HUMAN; HEMANGIOMA, CAVERNOUS; HUMAN; LINKAGE (GENETICS); MAGNETIC RESONANCE IMAGING; MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM (GENETICS); RECOMBINATION, GENETIC; REPETITIVE SEQUENCES, NUCLEIC ACID; SUPPORT, NON-U.S. GOV'T;

EID: 0029020926     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.92.14.6620     Document Type: Article

References (33)