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Volumn 85, Issue 12, 2006, Pages 883-885

Fluorescence in situ hybridization using the subtelomeric 11q probe as a diagnostic tool for congenital thrombocytopenia [5]

(7) Göhring, Gudrun a Hanke, C b Kratz, C b Kontny, U b Steinemann, D a Niemeyer, C M b Schlegelberger, B a

a HANNOVER MEDICAL SCHOOL (Germany)

b UNIVERSITY OF FREIBURG (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ATM PROTEIN;

BONE MARROW CELL; BRAIN HEMORRHAGE; CASE REPORT; CHROMOSOME 11Q; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME BANDING PATTERN; CHROMOSOME DELETION; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; JACOBSEN SYNDROME; KARYOTYPE; LETTER; MOLECULAR PROBE; NEWBORN; PRIORITY JOURNAL; THROMBOCYTE COUNT; THROMBOCYTE TRANSFUSION; THROMBOCYTOPENIA;

CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 11; DNA PROBES; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; THROMBOCYTOPENIA;

EID: 33750133985 PISSN: 09395555 EISSN: None Source Type: Journal
DOI: 10.1007/s00277-006-0177-2 Document Type: Letter

Times cited : (5)

References (6)

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2
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- Clinical and molecular characterization of patients with distal 11q deletions
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3
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- The 11q terminal deletion disorder: A prospective study of 110 cases
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4
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- Localization of Jacobsen syndrome breakpoints on a 40-Mb physical map of distal chromosome 11q
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5
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- Micromegakaryocytes in a patient with partial deletion of the long arm of chromosome 11 [del(11)(q24.2qter)] and chronic thrombocytopenic purpura
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6
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- Jacobsen syndrome and Beckwith-Wiedemann syndrome caused by a parental pericentric inversion inv(11)(p15q24)
- (in press). DOI 10.1111/j.1469-1809.2006.00271.x
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