ROR2 is mutated in hereditary brachydactyly with nail dysplasia, but not in Sorsby syndrome [5]

Clinical Genetics

Volumn 64, Issue 3, 2003, Pages 263-265

  Goodman, Frances ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE; GUANINE; PROTEIN ROR2; PROTEIN TYROSINE KINASE; TRYPTOPHAN; UNCLASSIFIED DRUG;

ALLELE; BRACHYDACTYLY; CHROMOSOME 9Q; CODON; COLOBOMA; EXON; FAMILY STUDY; GENE MUTATION; GENE SEQUENCE; GENETIC LINKAGE; GENITAL MALFORMATION; GERMANY; HEARING LOSS; HETEROZYGOSITY; HUMAN; KIDNEY AGENESIS; LETTER; NAIL DYSPLASIA; NONSENSE MUTATION; PRIORITY JOURNAL; RESTRICTION MAPPING;

ABNORMALITIES, MULTIPLE; COLOBOMA; FEMALE; FINGERS; FOOT DEFORMITIES, CONGENITAL; GENES, DOMINANT; HUMANS; LIMB DEFORMITIES, CONGENITAL; MACULA LUTEA; MALE; NAILS, MALFORMED; NOSE; PEDIGREE; RECEPTORS, CELL SURFACE; SYNDROME; TOOTH ABNORMALITIES; WALES;

EID: 0042914398     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2003.00139.x     Document Type: Letter

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