Your search returned 12 results.

Results
	1.	cis-regulatory mutations are a genetic cause of human limb malformations. [electronic resource] by VanderMeer, Julia E Ahituv, Nadav Producer: 20110922 In: Developmental dynamics : an official publication of the American Association of Anatomists vol. 240 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Genome-wide identification of signaling center enhancers in the developing limb. [electronic resource] by VanderMeer, Julia E Smith, Robin P Jones, Stacy L Ahituv, Nadav Producer: 20141230 In: Development (Cambridge, England) vol. 141 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel ZRS mutation in a Balochi tribal family with triphalangeal thumb, pre-axial polydactyly, post-axial polydactyly, and syndactyly. [electronic resource] by VanderMeer, Julia E Afzal, Muhammad Alyas, Saadia Haque, Sayedul Ahituv, Nadav Malik, Sajid Producer: 20121105 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)
	4.	Human developmental enhancers conserved between deuterostomes and protostomes. [electronic resource] by Clarke, Shoa L VanderMeer, Julia E Wenger, Aaron M Schaar, Bruce T Ahituv, Nadav Bejerano, Gill Producer: 20121217 In: PLoS genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A novel ZRS mutation leads to preaxial polydactyly type 2 in a heterozygous form and Werner mesomelic syndrome in a homozygous form. [electronic resource] by VanderMeer, Julia E Lozano, Reymundo Sun, Miao Xue, Yuan Daentl, Donna Jabs, Ethylin Wang Wilcox, William R Ahituv, Nadav Producer: 20150330 In: Human mutation vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A novel 13 base pair insertion in the sonic hedgehog ZRS limb enhancer (ZRS/LMBR1) causes preaxial polydactyly with triphalangeal thumb. [electronic resource] by Laurell, Tobias Vandermeer, Julia E Wenger, Aaron M Grigelioniene, Giedre Nordenskjöld, Agneta Arner, Marianne Ekblom, Anna Gerber Bejerano, Gill Ahituv, Nadav Nordgren, Ann Producer: 20120927 In: Human mutation vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Bat Accelerated Regions Identify a Bat Forelimb Specific Enhancer in the HoxD Locus. [electronic resource] by Booker, Betty M Friedrich, Tara Mason, Mandy K VanderMeer, Julia E Zhao, Jingjing Eckalbar, Walter L Logan, Malcolm Illing, Nicola Pollard, Katherine S Ahituv, Nadav Producer: 20160808 In: PLoS genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study population. [electronic resource] by Carter, Tonia C Pangilinan, Faith Troendle, James F Molloy, Anne M VanderMeer, Julia Mitchell, Adam Kirke, Peadar N Conley, Mary R Shane, Barry Scott, John M Brody, Lawrence C Mills, James L Producer: 20110517 In: American journal of medical genetics. Part A vol. 155A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Identification of three novel FGF16 mutations in X-linked recessive fusion of the fourth and fifth metacarpals and possible correlation with heart disease. [electronic resource] by Laurell, Tobias Nilsson, Daniel Hofmeister, Wolfgang Lindstrand, Anna Ahituv, Nadav Vandermeer, Julia Amilon, Anders Annerén, Göran Arner, Marianne Pettersson, Maria Jäntti, Nina Rosberg, Hans-Eric Cattini, Peter A Nordenskjöld, Agneta Mäkitie, Outi Grigelioniene, Giedre Nordgren, Ann Producer: 20141021 In: Molecular genetics & genomic medicine vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Evaluation of proton-coupled folate transporter (SLC46A1) polymorphisms as risk factors for neural tube defects and oral clefts. [electronic resource] by VanderMeer, Julia E Carter, Tonia C Pangilinan, Faith Mitchell, Adam Kurnat-Thoma, Emma Kirke, Peadar N Troendle, James F Molloy, Anne M Munger, Ronald G Feldkamp, Marcia L Mansilla, Maria A Mills, James L Murray, Jeff C Brody, Lawrence C Producer: 20161213 In: American journal of medical genetics. Part A vol. 170A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Transcriptomic and epigenomic characterization of the developing bat wing. [electronic resource] by Eckalbar, Walter L Schlebusch, Stephen A Mason, Mandy K Gill, Zoe Parker, Ash V Booker, Betty M Nishizaki, Sierra Muswamba-Nday, Christiane Terhune, Elizabeth Nevonen, Kimberly A Makki, Nadja Friedrich, Tara VanderMeer, Julia E Pollard, Katherine S Carbone, Lucia Wall, Jeff D Illing, Nicola Ahituv, Nadav Producer: 20170530 In: Nature genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects. [electronic resource] by Pangilinan, Faith Molloy, Anne M Mills, James L Troendle, James F Parle-McDermott, Anne Signore, Caroline O'Leary, Valerie B Chines, Peter Seay, Jessica M Geiler-Samerotte, Kerry Mitchell, Adam VanderMeer, Julia E Krebs, Kristine M Sanchez, Angelica Cornman-Homonoff, Joshua Stone, Nicole Conley, Mary Kirke, Peadar N Shane, Barry Scott, John M Brody, Lawrence C Producer: 20130103 In: BMC medical genetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)