High-resolution physical and genetic mapping of the critical region for Meckel syndrome and Mulibrey Nanism on chromosome 17q22-q23

Genome Research

Volumn 9, Issue 3, 1999, Pages 267-276

  Paavola, Paulina ^a,b   Avela, Kristiina ^b,c   Horelli Kuitunen, Nina ^d   Bärlund, Maarit ^e   Kallioniemi, Anne ^e   Idänheimo, Niina ^b,c   Kyttälä, Mira ^a,b   De La Chapelle, Albert ^c,f   Palotie, Aarno ^d   Lehesjoki, Anna Elina ^b,c   Peltonen, Leena ^a,b  

^a NATIONAL PUBLIC HEALTH INSTITUTE   (Finland)

^b UNIVERSITY OF HELSINKI   (Finland)

^c FOLKHÄLSAN INSTITUTE OF GENETICS   (Finland)

^d UNIVERSITY OF HELSINKI   (Finland)

^e NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^f OHIO STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 17Q; DWARFISM; EXPRESSED SEQUENCE TAG; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE MAPPING; MECKEL SYNDROME; MOLECULAR CLONING; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; DNA-BINDING PROTEINS; DWARFISM; ENCEPHALOCELE; GENES, RECESSIVE; HUMANS; LINKAGE DISEQUILIBRIUM; MENINGOCELE; MOLECULAR SEQUENCE DATA; PHYSICAL CHROMOSOME MAPPING; POLYCYSTIC KIDNEY, AUTOSOMAL RECESSIVE; POLYDACTYLY; SYNDROME; T-BOX DOMAIN PROTEINS;

BACTERIA (MICROORGANISMS);

EID: 0032921638     PISSN: 10889051     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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