The use of arrays to detect copy-number variations in clinical practice

Human Mutation

Volumn 33, Issue 6, 2012, Pages 905-

  Sikkema Raddatz, Birgit ^a   Sijmons, Rolf H ^a  

^a UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CANCER CELL; CHROMOSOME ABERRATION; CLINICAL PRACTICE; COPY NUMBER VARIATION; COPY NUMBER VARIATION ARRAY; CYTOGENETICS; EDITORIAL; GENETIC ANALYSIS; GENETIC SCREENING; HOMOZYGOSITY; HUMAN; KARYOTYPING; MEDICAL ETHICS; OUTCOME ASSESSMENT; PRACTICE GUIDELINE; PRIORITY JOURNAL; QUALITY CONTROL;

DNA COPY NUMBER VARIATIONS; HUMANS; MOLECULAR DIAGNOSTIC TECHNIQUES; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS;

EID: 84865171059     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.22084     Document Type: Editorial

References (5)

1. de Leeuw N, Dijkhuizen T, Hehir-Kwa JY, Carter NP, Feuk L, Firth HV, Kuhn RM, Ledbetter DH, Lese Martin C, van Ravenswaaij-Arts CMA, Scherer SW, Shams S, and others. 2012. Diagnostic interpretation of array data using public databases and internet sources. Hum Mutat 33:930-940.
2. Dondorp W, Sikkema-Raddatz B, de Die-Smulders C, de Wert G. 2012. Arrays in postnatal and prenatal diagnosis: an exploration of the ethics of consent. Hum Mutat 33:916-922.
3. Simons A, Sikkema-Raddatz B, de Leeuw N, Konrad NC, Hastings RJ, Schoumans J. 2012. Genome-wide array in routine diagnostics of hematological malignancies. Hum Mutat 33:941-948.
4. Vermeesch JR, Brady PD, Sanlaville D, Kok K, Hastings RJ. 2012. Genome-wide arrays: quality criteria and platforms to be used in routine diagnostics. Hum Mutat 33:906-915.
5. Vetro A, Bouman K, Hastings RJ, McMullan DJ, Vermeesch JR, Miller K, Sikkema-Raddatz B, Ledbetter D, Zuffardi O, van Ravenswaaij-Arts CMA. 2012. The introduction of arrays inprenatal diagnosis: a special challenge. Hum Mutat 33:923-929.