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	121.	A rare subtelomeric deletion syndrome: Wolf Hirschhorn syndrome. [electronic resource] by Zorlu, P Eksioglu, A S Ozkan, M Tos, T Senel, S Producer: 20141211 In: Genetic counseling (Geneva, Switzerland) vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	122.	A cryptic unbalanced translocation der(4)t(4;17)(p16.1;q25.3) identifies Wittwer syndrome as a variant of Wolf-Hirschhorn syndrome. [electronic resource] by Wieland, Ilse Schanze, Denny Schanze, Ina Volleth, Marianne Muschke, Petra Zenker, Martin Producer: 20150710 In: American journal of medical genetics. Part A vol. 164A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	123.	Review of accessory tragus with highlights of its associated syndromes. [electronic resource] by Bahrani, Bahar Khachemoune, Amor Producer: 20150730 In: International journal of dermatology vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	124.	Wolf-Hirschhorn syndrome (WHS) - literature review on the features of the syndrome. [electronic resource] by Paradowska-Stolarz, Anna M Producer: 20140930 In: Advances in clinical and experimental medicine : official organ Wroclaw Medical University vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	125.	Developmental delay and failure to thrive associated with a loss-of-function variant in WHSC1 (NSD2). [electronic resource] by Boczek, Nicole J Lahner, Carrie A Nguyen, Thuy-Mi Ferber, Matthew J Hasadsri, Linda Thorland, Erik C Niu, Zhiyv Gavrilova, Ralitza H Producer: 20191029 In: American journal of medical genetics. Part A vol. 176 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	126.	Phenocopy of Wolf-Hirschhorn syndrome in a patient with duplication 12q13.3q14.1. [electronic resource] by Dallapiccola, Bruno Bernardini, Laura Novelli, Antonio Mingarelli, Rita Producer: 20090416 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	127.	Interstitial microdeletion of 4p16.3: contribution of WHSC1 haploinsufficiency to the pathogenesis of developmental delay in Wolf-Hirschhorn syndrome. [electronic resource] by Izumi, Kosuke Okuno, Hironobu Maeyama, Katsuhiro Sato, Seiji Yamamoto, Toshiyuki Torii, Chiharu Kosaki, Rika Takahashi, Takao Kosaki, Kenjiro Producer: 20100708 In: American journal of medical genetics. Part A vol. 152A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	128.	Submicroscopic duplication of the Wolf-Hirschhorn critical region with a 4p terminal deletion. [electronic resource] by Roselló, M Monfort, S Orellana, C Ferrer-Bolufer, I Quiroga, R Oltra, S Martínez, F Producer: 20090917 In: Cytogenetic and genome research vol. 125 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	129.	Microarray and FISH-based genotype-phenotype analysis of 22 Japanese patients with Wolf-Hirschhorn syndrome. [electronic resource] by Shimizu, Kenji Wakui, Keiko Kosho, Tomoki Okamoto, Nobuhiko Mizuno, Seiji Itomi, Kazuya Hattori, Shigeto Nishio, Kimio Samura, Osamu Kobayashi, Yoshiyuki Kako, Yuko Arai, Takashi Tsutomu, Oh-ishi Kawame, Hiroshi Narumi, Yoko Ohashi, Hirofumi Fukushima, Yoshimitsu Producer: 20141103 In: American journal of medical genetics. Part A vol. 164A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	130.	Developmental trajectories in syndromes with intellectual disability, with a focus on Wolf-Hirschhorn and its cognitive-behavioral profile. [electronic resource] by Fisch, Gene S Carpenter, Nancy Howard-Peebles, Patricia N Holden, Jeanette J A Tarleton, Jack Simensen, Richard Battaglia, Agatino Producer: 20120615 In: American journal on intellectual and developmental disabilities vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	131.	Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder. [electronic resource] by Zollino, Marcella Orteschi, Daniela Ruiter, Mariken Pfundt, Rolph Steindl, Katharina Cafiero, Concetta Ricciardi, Stefania Contaldo, Ilaria Chieffo, Daniela Ranalli, Domiziana Acquafondata, Celeste Murdolo, Marina Marangi, Giuseppe Asaro, Alessia Battaglia, Domenica Producer: 20140813 In: Epilepsia vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	132.	De novo unbalanced translocation (4p duplication/8p deletion) in a patient with autism, OCD, and overgrowth syndrome. [electronic resource] by Sagar, Angela Pinto, Dalila Najjar, Fedra Guter, Stephen J Macmillan, Carol Cook, Edwin H Producer: 20171201 In: American journal of medical genetics. Part A vol. 173 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	133.	[Prenatal diagnosis of a case with combined Wolf-Hirschhorn syndrome and Jacobsen syndrome]. [electronic resource] by Dong, Yanling Hu, Huamei Hu, Hua Zhang, Rong Hu, Bin Long, Yang Xu, Gang Yao, Hong Producer: 20151116 In: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	134.	Clinical features in adult patient with Wolf-Hirschhorn syndrome. [electronic resource] by Martínez-Quintana, E Rodríguez-González, F Producer: 20150120 In: Morphologie : bulletin de l'Association des anatomistes vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	135.	Deletions involving genes WHSC1 and LETM1 may be necessary, but are not sufficient to cause Wolf-Hirschhorn Syndrome. [electronic resource] by Andersen, Erica F Carey, John C Earl, Dawn L Corzo, Deyanira Suttie, Michael Hammond, Peter South, Sarah T Producer: 20141118 In: European journal of human genetics : EJHG vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	136.	Detection of recurrent 4p16.3 microdeletion with 2p25.3 microduplication by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in a fetus from a family with Wolf-Hirschhorn syndrome. [electronic resource] by Yang, Wen-Xu Pan, Hong Wang, Song-Tao Li, Lin Wu, Hai-Rong Qi, Yu Producer: 20170109 In: Taiwanese journal of obstetrics & gynecology vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	137.	Inv dup del(4)(:p13-->p16.3::p16.3-->qter) in a girl without typical manifestations of Wolf-Hirschhorn syndrome. [electronic resource] by Paskulin, Giorgio A Riegel, Mariluce Cotter, Philip D Kiss, Andrea Rosa, Rafael F M Zen, Paulo R G Mombach, Rômulo Graziadio, Carla Producer: 20090730 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	138.	A histone H3 lysine 36 trimethyltransferase links Nkx2-5 to Wolf-Hirschhorn syndrome. [electronic resource] by Nimura, Keisuke Ura, Kiyoe Shiratori, Hidetaka Ikawa, Masato Okabe, Masaru Schwartz, Robert J Kaneda, Yasufumi Producer: 20090902 In: Nature vol. 460 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	139.	Auditory hair cell defects as potential cause for sensorineural deafness in Wolf-Hirschhorn syndrome. [electronic resource] by Ahmed, Mohi Ura, Kiyoe Streit, Andrea Producer: 20160726 In: Disease models & mechanisms vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	140.	A novel 4p16.3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic features. [electronic resource] by Cyr, Andrew B Nimmakayalu, Manjunath Longmuir, Susannah Q Patil, Shivanand R Keppler-Noreuil, Kim M Shchelochkov, Oleg A Producer: 20120209 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)

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Your search returned 163 results.