Delineation of complex chromosomal rearrangements: Evidence for increased complexity

Human Genetics

Volumn 114, Issue 5, 2004, Pages 448-457

  Astbury, Caroline ^a   Christ, Laurie A ^a   Aughton, David J ^b   Cassidy, Suzanne B ^c,h   Fujimoto, Atsuko ^d   Pletcher, Beth A ^e   Schafer, Irwin A ^f   Schwartz, Stuart ^a,g  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b WILLIAM BEAUMONT HOSPITAL   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d LAC USC MEDICAL CENTER   (United States)

^e RUTGERS NEW JERSEY MEDICAL SCHOOL   (United States)

^f METROHEALTH MEDICAL CENTER   (United States)

^g Center for Human Genetics   (United States)

^h Medical Center   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANIRIDIA; ARTICLE; ATTENTION DEFICIT DISORDER; BACTERIAL ARTIFICIAL CHROMOSOME; BRAIN DISEASE; CASE REPORT; CHONDROMATOSIS; CHROMOSOME ANALYSIS; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOME REARRANGEMENT; CONGENITAL HEART MALFORMATION; DATA ANALYSIS; DEVELOPMENTAL DISORDER; FACE MALFORMATION; FAILURE TO THRIVE; FEEDING DISORDER; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GAZE; GENE DISRUPTION; HAND MALFORMATION; HEART DISEASE; HEART VENTRICLE SEPTUM DEFECT; HEREDITARY MULTIPLE EXOSTOSIS; HUMAN; HUMAN CELL; KIDNEY POLYCYSTIC DISEASE; LEARNING DISORDER; LETHARGY; MALE; MEDICAL GENETICS; MENTAL DEFICIENCY; MICROCEPHALY; MOTOR DYSFUNCTION; MUSCLE HYPOTONIA; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; PRECOCIOUS PUBERTY; PRESCHOOL CHILD; PRIORITY JOURNAL; PULMONARY VALVE STENOSIS; RESPIRATORY DISTRESS; SEIZURE; SPEECH DISORDER; TERATOLOGY; CELL LINE; CHROMOSOME ABERRATION; CHROMOSOME BANDING PATTERN; CHROMOSOME DISORDER; COMPARATIVE STUDY; COSMID; GENE REARRANGEMENT; GENETICS; KARYOTYPING; MULTIPLE MALFORMATION SYNDROME;

ABNORMALITIES, MULTIPLE; ADULT; CELL LINE; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOME DISORDERS; CHROMOSOMES, ARTIFICIAL, BACTERIAL; COSMIDS; FEMALE; GENE REARRANGEMENT; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; MALE;

EID: 2542482661     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-003-1079-1     Document Type: Article

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