Modification of risk for cancer as a coincidental finding in DNA array investigation. [electronic resource]

By:

Rostasy, K

Contributor(s):

Fauth, C
Gautsch, K
Laimer, I
Krabichler, B
Wimmer, K
Frühmesser, A
Kotzot, D
Moshir, S

Producer: 20130827Description: 284-7 p. digitalISSN:

1399-0004

Subject(s):

Adolescent
Checkpoint Kinase 2
Chromosome Deletion
Chromosome Disorders -- diagnosis
Chromosomes, Human, Pair 22 -- genetics
Female
Humans
Incidental Findings
Magnetic Resonance Imaging
Neurofibromin 2 -- genetics
Neuroma, Acoustic -- diagnosis
Oligonucleotide Array Sequence Analysis -- methods
Protein Serine-Threonine Kinases -- genetics
Risk Factors

Online resources:

Available from publisher's website

In: Clinical genetics vol. 83

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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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Modification of risk for cancer as a coincidental finding in DNA array investigation.

APA

Rostasy K., Fauth C., Gautsch K., Laimer I., Krabichler B., Wimmer K., Frühmesser A., Kotzot D. & Moshir S. (20130827). Modification of risk for cancer as a coincidental finding in DNA array investigation. : Clinical genetics.

Chicago

Rostasy K, Fauth C, Gautsch K, Laimer I, Krabichler B, Wimmer K, Frühmesser A, Kotzot D and Moshir S. 20130827. Modification of risk for cancer as a coincidental finding in DNA array investigation. : Clinical genetics.

Harvard

Rostasy K., Fauth C., Gautsch K., Laimer I., Krabichler B., Wimmer K., Frühmesser A., Kotzot D. and Moshir S. (20130827). Modification of risk for cancer as a coincidental finding in DNA array investigation. : Clinical genetics.

MLA

Rostasy K, Fauth C, Gautsch K, Laimer I, Krabichler B, Wimmer K, Frühmesser A, Kotzot D and Moshir S. Modification of risk for cancer as a coincidental finding in DNA array investigation. : Clinical genetics. 20130827.

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