Exclusive paternal origin of new mutations in Apert syndrome

Nature Genetics

Volumn 13, Issue 1, 1996, Pages 48-53

  Moloney, Dominique M ^a,b   Slaney, Sarah F ^a,b,c   Oldridge, Michael ^a   Wall, Steven A ^b   Sahlin, Pelle ^d   Stenman, Göran ^d,e   Wilkie, Andrew O M ^a,b,c  

^a JOHN RADCLIFFE HOSPITAL   (United Kingdom)

^b RADCLIFFE INFIRMARY   (United Kingdom)

^c OXFORD UNIVERSITY HOSPITALS NHS FOUNDATION TRUST   (United Kingdom)

^d UNIVERSITY OF GOTHENBURG   (Sweden)

^e LINKÖPING UNIVERSITY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ACROCEPHALOSYNDACTYLY; ARTICLE; GENE MUTATION; HUMAN; NUCLEIC ACID BASE SUBSTITUTION; PATERNAL AGE; PATHOGENESIS; PRIORITY JOURNAL; Y CHROMOSOMAL INHERITANCE;

ACROCEPHALOSYNDACTYLIA; ADULT; BASE SEQUENCE; CYTOSINE; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; FATHERS; FEMALE; GENE FREQUENCY; GENOMIC IMPRINTING; GENOTYPE; GUANINE; HAPLOTYPES; HUMANS; MALE; MATERNAL AGE; MODELS, GENETIC; MOLECULAR SEQUENCE DATA; PATERNAL AGE; PEDIGREE; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; RECEPTOR PROTEIN-TYROSINE KINASES; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 2; RECEPTORS, FIBROBLAST GROWTH FACTOR; RESTRICTION MAPPING; VARIATION (GENETICS);

EID: 0029983638     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0596-48     Document Type: Article

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