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	1.	Positional cloning of the s haplotype determining the floral and incompatibility phenotype of the long-styled morph of distylous Turnera subulata. [electronic resource] by Labonne, Jonathan D J Shore, Joel S Producer: 20110222 In: Molecular genetics and genomics : MGG vol. 285 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Changes in nucleosome position at transcriptional start sites of specific genes in Zea mays mediator of paramutation1 mutants. [electronic resource] by Labonne, Jonathan D J Dorweiler, Jane E McGinnis, Karen M Producer: 20150511 In: Epigenetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A microdeletion encompassing PHF21A in an individual with global developmental delay and craniofacial anomalies. [electronic resource] by Labonne, Jonathan D J Vogt, Julie Reali, Lisa Kong, Il-Keun Layman, Lawrence C Kim, Hyung-Goo Producer: 20161017 In: American journal of medical genetics. Part A vol. 167A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Comparative deletion mapping at 1p31.3-p32.2 implies NFIA responsible for intellectual disability coupled with macrocephaly and the presence of several other genes for syndromic intellectual disability. [electronic resource] by Labonne, Jonathan D J Shen, Yiping Kong, Il-Keun Diamond, Michael P Layman, Lawrence C Kim, Hyung-Goo Producer: 20160321 In: Molecular cytogenetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	The long and short of the S-locus in Turnera (Passifloraceae). [electronic resource] by Shore, Joel S Hamam, Hasan J Chafe, Paul D J Labonne, Jonathan D J Henning, Paige M McCubbin, Andrew G Producer: 20200722 In: The New phytologist vol. 224 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A microdeletion at Xq22.2 implicates a glycine receptor GLRA4 involved in intellectual disability, behavioral problems and craniofacial anomalies. [electronic resource] by Labonne, Jonathan D J Graves, Tyler D Shen, Yiping Jones, Julie R Kong, Il-Keun Layman, Lawrence C Kim, Hyung-Goo Producer: 20161230 In: BMC neurology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Concomitant partial exon skipping by a unique missense mutation of RPS6KA3 causes Coffin-Lowry syndrome. [electronic resource] by Labonne, Jonathan D J Chung, Min Ji Jones, Julie R Anand, Priya Wenzel, Wolfgang Iacoboni, Daniela Layman, Lawrence C Kim, Hyung-Goo Producer: 20160225 In: Gene vol. 575 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability. [electronic resource] by Labonne, Jonathan D J Lee, Kang-Han Iwase, Shigeki Kong, Il-Keun Diamond, Michael P Layman, Lawrence C Kim, Cheol-Hee Kim, Hyung-Goo Producer: 20170621 In: Human genetics vol. 135 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Steric Clash in the SET Domain of Histone Methyltransferase NSD1 as a Cause of Sotos Syndrome and Its Genetic Heterogeneity in a Brazilian Cohort. [electronic resource] by Ha, Kyungsoo Anand, Priya Lee, Jennifer A Jones, Julie R Kim, Chong Ae Bertola, Debora Romeo Labonne, Jonathan D J Layman, Lawrence C Wenzel, Wolfgang Kim, Hyung-Goo Publication details: Genes Nov 2016 In: Genes vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Comparative Genomic Mapping Implicates LRRK2 for Intellectual Disability and Autism at 12q12, and HDHD1, as Well as PNPLA4, for X-Linked Intellectual Disability at Xp22.31. [electronic resource] by Labonne, Jonathan D J Driessen, Terri M Harris, Marvin E Kong, Il-Keun Brakta, Soumia Theisen, John Sangare, Modibo Layman, Lawrence C Kim, Cheol-Hee Lim, Janghoo Kim, Hyung-Goo Publication details: Journal of clinical medicine Jan 2020 In: Journal of clinical medicine vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)