Phenotypic definition of chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15

American Journal of Medical Genetics, Part A

Volumn 140, Issue 24, 2006, Pages 2776-2785

  Boyles, Abee L ^a   Enterline, David S ^a   Hammock, Preston H ^a   Siegel, Deborah G ^a   Slifer, Susan H ^a   Mehltretter, Lorraine ^a   Gilbert, John R ^a   Hu Lince, Diane ^b   Stephan, Dietrich ^b   Batzdorf, Ulrich ^c   Benzel, Edward ^d   Ellenbogen, Richard ^e   Green, Barth A ^f   Kula, Roger ^g   Menezes, Arnold ^h   Mueller, Diane ⁱ   Oro, John J ⁱ   Iskandar, Bermans J ^j   George, Timothy M ^a   Milhorat, Thomas H ^k   Speer, Marcy C ^a   more..

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b TRANSLATIONAL GENOMICS RESEARCH INSTITUTE   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d LERNER RESEARCH INSTITUTE   (United States)

^e UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^f UNIVERSITY OF MIAMI   (United States)

^g Chiari Institute   (United States)

^h UNIVERSITY OF IOWA HOSPITALS AND CLINICS   (United States)

ⁱ UNIVERSITY OF MISSOURI   (United States)

^j UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

^k NORTH SHORE UNIVERSITY HOSPITAL   (United States)

more..

Author keywords

Chiari type I malformation; Cranial morphology; Genome wide linkage screen

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BRAIN HERNIA; BRAIN MALFORMATION; BRAIN SIZE; CEREBELLUM; CHIARI FROMMEL SYNDROME; CHILD; CHROMOSOME 15; CHROMOSOME 9; CORRELATION ANALYSIS; FEMALE; FIBRILLIN 1 GENE; FORAMEN MAGNUM; GENE; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC SCREENING; GENOME ANALYSIS; HERITABILITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MARFAN SYNDROME; NEUROLOGIC DISEASE; NUCLEAR MAGNETIC RESONANCE IMAGING; POSTERIOR FOSSA; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL ANALYSIS; STATISTICAL SIGNIFICANCE;

ARNOLD-CHIARI MALFORMATION; CEREBELLUM; CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, PAIR 9; CRANIAL FOSSA, POSTERIOR; FEMALE; FORAMEN MAGNUM; GENETIC SCREENING; GENOTYPE; HUMANS; LINKAGE (GENETICS); LOD SCORE; MAGNETIC RESONANCE IMAGING; MALE; PEDIGREE; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 33845270402     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.31546     Document Type: Article

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