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	1.	Mutations of NANOS1, a human homologue of the Drosophila morphogen, are associated with a lack of germ cells in testes or severe oligo-astheno-teratozoospermia. [electronic resource] by Kusz-Zamelczyk, Kamila Sajek, Marcin Spik, Anna Glazar, Renata Jędrzejczak, Piotr Latos-Bieleńska, Anna Kotecki, Maciej Pawelczyk, Leszek Jaruzelska, Jadwiga Producer: 20131125 In: Journal of medical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Whole exome sequencing identifies FGF16 nonsense mutations as the cause of X-linked recessive metacarpal 4/5 fusion. [electronic resource] by Jamsheer, Aleksander Zemojtel, Tomasz Kolanczyk, Mateusz Stricker, Sigmar Hecht, Jochen Krawitz, Peter Doelken, Sandra C Glazar, Renata Socha, Magdalena Mundlos, Stefan Producer: 20140508 In: Journal of medical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland. [electronic resource] by Wozniak, Anna Wolnik-Brzozowska, Danuta Wisniewska, Marzena Glazar, Renata Materna-Kiryluk, Anna Moszura, Tomasz Badura-Stronka, Magdalena Skolozdrzy, Joanna Krawczynski, Maciej R Zeyland, Joanna Bobkowski, Waldemar Slomski, Ryszard Latos-Bielenska, Anna Siwinska, Aldona Producer: 20110810 In: BMC pediatrics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)