Exclusion of allelism of noonan syndrome and neurofibromatosis-type 1 in a large family with noonan syndrome-neurofibromatosis association

American Journal of Medical Genetics

Volumn 66, Issue 3, 1996, Pages 347-355

  Bahuau, Michel ^a,b   Flintoff, Wayne ^a,d   Assouline, Brigitte ^b   Lyonnet, Stanislas ^a   Le Merrer, Martine ^a   Prieur, Marguerite ^c   Guilloud Bataille, Michel ^a   Feingold, Nicole ^a   Munnich, Arnold ^a   Vidaud, Michel ^b   Vidaud, Dominique ^b  

^a INSERM   (France)

^b UNIVERSITÉ PARIS DESCARTES   (France)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

^d UNIVERSITY OF WESTERN ONTARIO   (Canada)

Author keywords

clinical association; linkage exclusion; neurofibromatosis type 1; Noonan syndrome

Indexed keywords

DNA;

ALLELISM; ARTICLE; CASE REPORT; DISEASE ASSOCIATION; DNA DETERMINATION; GENE MUTATION; GENETIC LINKAGE; HUMAN; HUMAN CELL; HUMAN TISSUE; INFANT; NEUROFIBROMATOSIS; NOONAN SYNDROME; PHENOTYPE; PRIORITY JOURNAL;

ALLELES; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; GENES, NEUROFIBROMATOSIS 1; GENETIC MARKERS; GENOTYPE; HUMANS; INFANT; LINKAGE (GENETICS); MALE; NEUROFIBROMATOSIS 1; NOONAN SYNDROME; PEDIGREE; PHENOTYPE; POLYMORPHISM, GENETIC;

EID: 0030456861     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19961218)66:3<347::AID-AJMG20>3.0.CO;2-L     Document Type: Article

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