A chromosome 10 variant with a 12 Mb inversion [inv(10)(q11.22q21.1)] identical by descent and frequent in the Swedish population

American Journal of Medical Genetics, Part A

Volumn 149, Issue 3, 2009, Pages 380-386

  Entesarian, Miriam ^a   Carlsson, Birgit ^a   Mansouri, Mahmoud Reza ^a   Stattin, Eva Lena ^b   Holmberg, Eva ^c   Golovleva, Irina ^b   Stefansson, Hreinn ^d   Klar, Joakim ^a   Dahl, Niklas ^a,e  

^a UPPSALA UNIVERSITY   (Sweden)

^b UMEÅ UNIVERSITY HOSPITAL   (Sweden)

^c SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

^d DECODE GENETICS   (Iceland)

^e UPPSALA UNIVERSITY   (Sweden)

Author keywords

Breakpoint cloning; Chromosome 10q; Founder effect; Paracentric inversion

Indexed keywords

AMNIOCENTESIS; ARTICLE; CENTROMERE; CHROMOSOME 10; CHROMOSOME ANALYSIS; CONTROLLED STUDY; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; GENE FREQUENCY; GENE MAPPING; GENE SEQUENCE; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; INTERSPERSED REPEAT; KARYOTYPE; MAJOR CLINICAL STUDY; MICROSATELLITE MARKER; MOLECULAR CLONING; PARACENTRIC CHROMOSOME INVERSION; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RETROSPECTIVE STUDY; SEQUENCE ANALYSIS; SOUTHERN BLOTTING;

AMNIOCENTESIS; CHI-SQUARE DISTRIBUTION; CHROMOSOME BREAKAGE; CHROMOSOMES, ARTIFICIAL, BACTERIAL; CHROMOSOMES, HUMAN, PAIR 10; CLONING, MOLECULAR; CYTOGENETIC ANALYSIS; GENE FREQUENCY; GENETIC MARKERS; GENETIC VARIATION; GEOGRAPHY; HAPLOTYPES; HETEROZYGOTE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INVERSION, CHROMOSOME; MICROSATELLITE REPEATS; POLYMERASE CHAIN REACTION; POPULATION GROUPS; SEQUENCE ANALYSIS, DNA; SWEDEN;

EID: 61749084099     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32663     Document Type: Article

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