A highly informative CA/GT repeat polymorphism in intron 38 of the human neurofibromatosis type 1 (NF1) gene

Human Genetics

Volumn 92, Issue 4, 1993, Pages 429-430

  Lázaro, Conxi ^a   Gaona, Antonia ^a   Xu, Ganfeng ^b   Weiss, Robert ^b   Estivill, Xavier ^a  

^a HOSPITAL UNIVERSITARI DE BELLVITGE   (Spain)

^b UNIVERSITY OF UTAH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; CHROMOSOME 17Q; DOMINANT INHERITANCE; GENETIC POLYMORPHISM; HETEROZYGOSITY; HUMAN; INTRON; NEUROFIBROMATOSIS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

ALLELES; BASE SEQUENCE; CHROMOSOMES, HUMAN, PAIR 17; DNA; GENE FREQUENCY; GENES, NEUROFIBROMATOSIS 1; GENETIC MARKERS; HUMAN; INTRONS; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; POLYMORPHISM (GENETICS); REPETITIVE SEQUENCES, NUCLEIC ACID; SUPPORT, NON-U.S. GOV'T;

EID: 0027434880     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/BF01247353     Document Type: Article

References (4)

1. Gene for von Recklinghausen neurofibromatosis in the pericentromeric region of chromosome 17
2. A major segment of the neurofirbromatosis type 1 gene: cDNA sequence, genomic structure and point mutations
3. The human homolog of murine Evi-2 lies between two von Recklinghausen neurofibromatosis translocations
4. Type 1 neurofibromato-sis gene: identification of a large transcript disrupted in three NF1 patients