A genetic study of neurofibromatosis 1 in south-western Ontario. I Population, familial segregation of phenotype, and molecular linkage

Journal of Medical Genetics

Volumn 28, Issue 11, 1991, Pages 746-751

  Rodenhiser, D I ^a,b   Coulter Mackie, M B ^a   Jung, J H ^a   Singh, S M ^a  

^a UNIVERSITY OF WESTERN ONTARIO   (Canada)

^b CHILDREN S HOSPITAL OF WESTERN ONTARIO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BIRTH ORDER; CANADA; DISEASE SEVERITY; DNA PROBE; FAMILY; FEMALE; GENETIC LINKAGE; HETEROZYGOSITY; HUMAN; INCIDENCE; MAJOR CLINICAL STUDY; MALE; MUTATION RATE; NEUROFIBROMATOSIS; PARENT; PHENOTYPE; POPULATION RESEARCH; PREVALENCE; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

DNA PROBES; FEMALE; GENETICS, POPULATION; HETEROZYGOTE; HUMAN; LINKAGE (GENETICS); MALE; NEUROFIBROMATOSIS 1; NUCLEIC ACID HYBRIDIZATION; ONTARIO; PHENOTYPE; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; SUPPORT, NON-U.S. GOV'T;

EID: 0025989439     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.28.11.746     Document Type: Article

References (0)