Large deletions and uniparental disomy detected by SNP arrays in adults with thoracic aortic aneurysms and dissections

American Journal of Medical Genetics, Part A

Volumn 152, Issue 9, 2010, Pages 2399-2405

  Prakash, Siddharth ^a   LeMaire, Scott A ^a,b   Bray, Molly ^a   Milewicz, Dianna M ^c   Belmont, John W ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b ST LUKE S EPISCOPAL HOSPITAL   (United States)

^c UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CD146 ANTIGEN;

ADULT; AGED; ANEURYSM SURGERY; AORTA DISSECTION; AORTOGRAPHY; BECKWITH WIEDEMANN SYNDROME; CHROMOSOME DELETION; CLINICAL ARTICLE; COMPUTER ASSISTED TOMOGRAPHY; CONTROLLED STUDY; DLK 1 GENE; DNA MICROARRAY; ECHOCARDIOGRAPHY; FEMALE; GENE; GENE EXPRESSION; HUMAN; KLF 14 GENE; LETTER; LOEYS DIETZ SYNDROME; MALE; MALFORMATION SYNDROME; MOSAICISM; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SILVER RUSSELL SYNDROME; SINGLE NUCLEOTIDE POLYMORPHISM; THORACIC AORTA ANEURYSM; TP 73 GENE; UNIPARENTAL DISOMY;

AGED; AGED, 80 AND OVER; AORTIC ANEURYSM, THORACIC; AORTIC RUPTURE; CHROMOSOMES, HUMAN; FEMALE; HUMANS; MALE; MIDDLE AGED; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE DELETION; UNIPARENTAL DISOMY;

EID: 77956112334     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33571     Document Type: Letter

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