Genetic and physical mapping of the McKusick-Kaufman syndrome

Human Molecular Genetics

Volumn 7, Issue 3, 1998, Pages 475-481

  Stone, Deborah L ^a   Agarwala, Richa ^a   Schäffer, Alejandro A ^a   Weber, James L ^b   Vaske, David ^b   Oda, Takaya ^a   Chandrasekharappa, Settara C ^a   Francomano, Clair A ^a,c   Biesecker, Leslie G ^a  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b MARSHFIELD CLINIC   (United States)

^c JOHNS HOPKINS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALAGILLE SYNDROME; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOME 20P; COMPUTER PROGRAM; CONGENITAL HEART DISEASE; DATA BASE; DEVELOPMENTAL DISORDER; FEMALE; GENEALOGY; HOMOZYGOSITY; HUMAN; HYDROMETROCOLPOS; MALE; MCKUSICK KAUFMAN SYNDROME; PEDIGREE; PENETRANCE; POLYDACTYLY; PRIORITY JOURNAL; TANDEM REPEAT;

ABNORMALITIES, MULTIPLE; FEMALE; GENOTYPE; HEART DEFECTS, CONGENITAL; HOMOZYGOTE; HUMANS; LINKAGE (GENETICS); MALE; NUCLEAR FAMILY; PEDIGREE; POLYDACTYLY; RECOMBINATION, GENETIC; SYNDROME; UTERINE DISEASES; VAGINAL DISEASES;

EID: 0031909968     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/7.3.475     Document Type: Article

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