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Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome

✍ Scribed by Montenegro, Luciana Ribeiro; Silveira, Leticia F.G.; Tusset, Cintia; de Castro, Margaret; Versiani, Beatriz R.; Latronico, Ana Claudia; Mendonca, Berenice Bilharinho; Trarbach, Ericka B.

Book ID: 120431293
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 575 KB
Volume: 100
Category: Article
ISSN: 1556-5653
DOI: 10.1016/j.fertnstert.2013.04.045

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