Constitutional RUNX1 deletion presenting as non-syndromic thrombocytopenia with myelodysplasia: 21q22 ITSN1 as a candidate gene in mental retardation

Leukemia Research

Volumn 34, Issue 1, 2010, Pages e8-

  van der Crabben, Saskia ^a   van Binsbergen, Ellen ^a   Ausems, Margreet ^a   Poot, Martin ^a   Bierings, Marc ^a   Buijs, Arjan ^a  

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

INTERSECTIN; INTERSECTIN 1; TRANSCRIPTION FACTOR RUNX1; UNCLASSIFIED DRUG;

BONE MARROW BIOPSY; CASE REPORT; CHILD; CHROMOSOME 21; CHROMOSOME ANALYSIS; CHROMOSOME G BAND; CONTROLLED STUDY; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENOTYPE; GRANULOPOIESIS; HUMAN; KARYOTYPE; KARYOTYPE 46,XY; LETTER; MALE; MEGAKARYOPOIESIS; MENTAL DEFICIENCY; MYELODYSPLASTIC SYNDROME; NUMERICAL CHROMOSOME ABERRATION; PHYSICAL EXAMINATION; PRESCHOOL CHILD; PRIORITY JOURNAL; THROMBOCYTOPENIA; UMBILICAL HERNIA;

EID: 73249129521     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.leukres.2009.06.030     Document Type: Letter

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