ICF syndrome: High variability of the chromosomal phenotype and association with classical Hodgkin lymphoma

American Journal of Medical Genetics, Part A

Volumn 143, Issue 17, 2007, Pages 2052-2057

  Schuetz, C ^a   Barbi, G ^a,b   Barth, T F E ^b   Hoenig, M ^a   Schulz, A ^a   Moeller P ^b   Smeets, D ^c   De Greef, J C ^d   Van Der Maarel, S M ^d   Vogel, W ^b   Debatin, K M ^a   Friedrich, W ^a  

^a UNIVERSITY HOSPITAL ULM   (Germany)

^b UNIVERSITY OF ULM   (Germany)

^c RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^d LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Centromeric heterochromatin instability; Hodgkin lymphoma; Hypomethylation; ICF syndrome; Neoplasia; Tumor

Indexed keywords

DNA; IMMUNOGLOBULIN;

ARTICLE; BRACHIAL PLEXUS; CASE REPORT; CHROMOSOME; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; COGNITIVE DEVELOPMENT; COMPUTER ASSISTED TOMOGRAPHY; DIAGNOSTIC ERROR; DISEASE ASSOCIATION; FACE DYSMORPHIA; FEMALE; GENETIC DISORDER; HEART ARREST; HEMIPLEGIA; HISTOPATHOLOGY; HODGKIN DISEASE; HUMAN; HYPERTELORISM; HYPOGAMMAGLOBULINEMIA; IMMUNOCHEMISTRY; IMMUNODEFICIENCY CENTROMERIC INSTABILITY FACIAL ANOMALY; LYMPHOCYTE; MALE; METAPHASE CHROMOSOME; MOTOR DEVELOPMENT; MUSCLE HYPOTONIA; PARAPLEGIA; PHENOTYPE; PHILTRUM; PRIORITY JOURNAL; PSYCHOMOTOR RETARDATION; SCHOOL; SCHOOL CHILD; TUMOR BIOPSY; CHILD; CLINICAL FEATURE; DNA DETERMINATION; FACE MALFORMATION; GENETIC VARIABILITY; HUMAN TISSUE; ICF SYNDROME; IMMUNE DEFICIENCY; METAPHASE;

CENTROMERE; CHILD; CHILD, PRESCHOOL; CHROMOSOMAL INSTABILITY; FACIAL BONES; FEMALE; HETEROCHROMATIN; HODGKIN DISEASE; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; MALE; PHENOTYPE; VARIATION (GENETICS);

EID: 34548316492     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.31885     Document Type: Article

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