Your search returned 2 results.

Results
	1.	3p14 deletion is a rare contiguous gene syndrome: report of 2 new patients and an overview of 14 patients. [electronic resource] by Dimitrov, B I Ogilvie, C Wieczorek, D Wakeling, E Sikkema-Raddatz, B van Ravenswaaij-Arts, C M A Josifova, D Producer: 20160219 In: American journal of medical genetics. Part A vol. 167 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Distal limb deficiencies, micrognathia syndrome, and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangements. [electronic resource] by Dimitrov, B I de Ravel, T Van Driessche, J de Die-Smulders, C Toutain, A Vermeesch, J R Fryns, J P Devriendt, K Debeer, P Producer: 20100506 In: Journal of medical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search