Your search returned 2 results.

Results
	1.	The importance of advanced parental age in the origin of neurofibromatosis type 1. [electronic resource] by Snajderova, Marta Riccardi, Vincent M Petrak, Borivoj Zemkova, Daniela Zapletalova, Jirina Mardesic, Tonko Petrakova, Alena Lanska, Vera Marikova, Tatiana Bendova, Sarka Havlovicova, Marketa Kaluzova, Marie Producer: 20120604 In: American journal of medical genetics. Part A vol. 158A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Homozygous EXOSC3 mutation c.92G→C, p.G31A is a founder mutation causing severe pontocerebellar hypoplasia type 1 among the Czech Roma. [electronic resource] by Schwabova, Jaroslava Brozkova, Dana Safka Petrak, Borivoj Mojzisova, Mahulena Pavlickova, Klara Haberlova, Jana Mrazkova, Lenka Hedvicakova, Petra Hornofova, Ludmila Kaluzova, Marie Fencl, Filip Krutova, Marcela Zamecnik, Josef Seeman, Pavel Producer: 20140806 In: Journal of neurogenetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search