Methods and systems for the detection of microdeletion and...

Details Methods and systems for the detection of microdeletion and... Methods and systems for the detection of microdeletion and...

C - Chemistry, Metallurgy

40

B

C40B 40/06 (2006.01) C12Q 1/68 (2006.01) C40B 30/00 (2006.01) C40B 30/04 (2006.01)

Patent

CA 2639530

Methods for diagnosing the presence or absence of a genetic disorder in a patient are provided, wherein the genetic disorder is associated with a chromosomal abnormality at 1q41q42 and/or 16p 11.2p 12.2, and wherein the genetic disorder is not Fryns syndrome or congenital diaphragmatic hernia (CDH). Materials, such as microarrays for use in microarray CGH, and kits for use in such methods are also provided.

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