Your search returned 5 results.

Results
	1.	Terminal microdeletions of 13q34 chromosome region in patients with intellectual disability: Delineation of an emerging new microdeletion syndrome. [electronic resource] by Reinstein, Eyal Liberman, Meytal Feingold-Zadok, Michal Tenne, Tamar Graham, John M Producer: 20170103 In: Molecular genetics and metabolism vol. 118 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Mutations in the NEB gene cause fetal akinesia/arthrogryposis multiplex congenita. [electronic resource] by Feingold-Zadok, Michal Chitayat, David Chong, Karen Injeyan, Marie Shannon, Patrick Chapmann, Daphne Maymon, Ron Pillar, Nir Reish, Orit Producer: 20170926 In: Prenatal diagnosis vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Two siblings with early infantile myoclonic encephalopathy due to mutation in the gene encoding mitochondrial glutamate/H+ symporter SLC25A22. [electronic resource] by Cohen, Rony Basel-Vanagaite, Lina Goldberg-Stern, Hadassah Halevy, Ayelet Shuper, Avinoam Feingold-Zadok, Michal Behar, Doron M Straussberg, Rachel Producer: 20150710 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Isolated fetal horseshoe kidney does not seem to increase the risk for abnormal chromosomal microarray results. [electronic resource] by Sagi-Dain, Lena Maya, Idit Falik-Zaccai, Tzipora Feingold-Zadok, Michal Lev, Dorit Yonath, Hagit Kaliner, Ehud Frumkin, Ayala Ben Shachar, Shay Singer, Amihood Producer: 20180918 In: European journal of obstetrics, gynecology, and reproductive biology vol. 222 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Expanding the mutational spectrum of CRLF1 in Crisponi/CISS1 syndrome. [electronic resource] by Piras, Roberta Chiappe, Francesca Torraca, Ilaria La Buers, Insa Usala, Gianluca Angius, Andrea Akin, Mustafa Ali Basel-Vanagaite, Lina Benedicenti, Francesco Chiodin, Elisabetta El Assy, Osama Feingold-Zadok, Michal Guibert, Javier Kamien, Benjamin Kasapkara, Ciğdem Seher Kiliç, Esra Boduroğlu, Koray Kurtoglu, Selim Manzur, Adnan Y Onal, Eray Esra Paderi, Enrica Roche, Carmen Herrero Tümer, Leyla Unal, Sezin Utine, Gülen Eda Zanda, Giovanni Zankl, Andreas Zampino, Giuseppe Crisponi, Giangiorgio Crisponi, Laura Rutsch, Frank Producer: 20150129 In: Human mutation vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)