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	4621.	Pregnancy after preimplantation genetic diagnosis for brachydactyly type B. [electronic resource] by Hellani, Ali Abu-Amero, Khaled Azouri, Joseph Al-Sharif, Hadeel Barblet, Hamish El-Akoum, Siham Producer: 20090226 In: Reproductive biomedicine online vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4622.	Deletion, insertion and stop codon mutations in vif genes of HIV-1 infecting slow progressor patients. [electronic resource] by Rangel, Héctor Rafael Garzaro, Domingo Rodríguez, Anny Karely Ramírez, Alvaro Hernán Ameli, Gladys Del Rosario Gutiérrez, Cristina Pujol, Flor Helene Producer: 20091130 In: Journal of infection in developing countries vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4623.	Four human breast cancer cell lines with biallelic inactivating alpha-catenin gene mutations. [electronic resource] by Hollestelle, Antoinette Elstrodt, Fons Timmermans, Mieke Sieuwerts, Anieta M Klijn, Jan G M Foekens, John A den Bakker, Michael A Schutte, Mieke Producer: 20101025 In: Breast cancer research and treatment vol. 122 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4624.	Genetic incorporation of unnatural amino acids into proteins in Mycobacterium tuberculosis. [electronic resource] by Wang, Feng Robbins, Scott Guo, Jiantao Shen, Weijun Schultz, Peter G Producer: 20100930 In: PloS one vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4625.	Novel PHEX nonsense mutation in a patient with X-linked hypophosphatemic rickets and review of current therapeutic regimens. [electronic resource] by Kienitz, T Ventz, M Kaminsky, E Quinkler, M Producer: 20111109 In: Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4626.	Functional splicing assay of DSPP mutations in hereditary dentin defects. [electronic resource] by Lee, K-E Lee, S-K Jung, S-E Lee, Zh Kim, J-W Producer: 20120126 In: Oral diseases vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4627.	MDM2 inhibitor nutlin-3a induces apoptosis and senescence in cutaneous T-cell lymphoma: role of p53. [electronic resource] by Manfé, Valentina Biskup, Edyta Johansen, Peter Kamstrup, Maria R Krejsgaard, Thorbjørn F Morling, Niels Wulf, Hans C Gniadecki, Robert Producer: 20120618 In: The Journal of investigative dermatology vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4628.	A novel PAX6 mutation in Chinese patients with severe congenital aniridia. [electronic resource] by He, Yan Pan, Zhiqiang Luo, Fei Producer: 20130124 In: Current eye research vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4629.	Dravet syndrome: seizure control and gait in adults with different SCN1A mutations. [electronic resource] by Rilstone, Jennifer J Coelho, Fernando M Minassian, Berge A Andrade, Danielle M Producer: 20121026 In: Epilepsia vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4630.	The VPS33B-binding protein VPS16B is required in megakaryocyte and platelet α-granule biogenesis. [electronic resource] by Urban, Denisa Li, Ling Christensen, Hilary Pluthero, Fred G Chen, Shao Zun Puhacz, Michael Garg, Parvesh M Lanka, Kiran K Cummings, James J Kramer, Helmut Wasmuth, James D Parkinson, John Kahr, Walter H A Producer: 20130228 In: Blood vol. 120 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4631.	Novel WDR72 mutation and cytoplasmic localization. [electronic resource] by Lee, S-K Seymen, F Lee, K-E Kang, H-Y Yildirim, M Tuna, E Bahar Gencay, K Hwang, Y-H Nam, K H De La Garza, R J Hu, J C-C Simmer, J P Kim, J-W Producer: 20101223 In: Journal of dental research vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4632.	A novel nonsense mutation in rhodopsin gene in two Indonesian families with autosomal recessive retinitis pigmentosa. [electronic resource] by Kartasasmita, Arief Fujiki, Keiko Iskandar, Erwin Sovani, Iwan Fujimaki, Takuro Murakami, Akira Producer: 20110429 In: Ophthalmic genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4633.	Accumulation of defective HIV-1 variants in a patient with slow disease progression. [electronic resource] by Paolucci, Stefania Gulminetti, Roberto Maserati, Renato Dossena, Luca Baldanti, Fausto Producer: 20110502 In: Current HIV research vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4634.	GJB1/Connexin 32 whole gene deletions in patients with X-linked Charcot-Marie-Tooth disease. [electronic resource] by Gonzaga-Jauregui, Claudia Zhang, Feng Towne, Charles F Batish, Sat Dev Lupski, James R Producer: 20110118 In: Neurogenetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4635.	CXCR4 WHIM-like frameshift and nonsense mutations promote ibrutinib resistance but do not supplant MYD88(L265P) -directed survival signalling in Waldenström macroglobulinaemia cells. [electronic resource] by Cao, Yang Hunter, Zachary R Liu, Xia Xu, Lian Yang, Guang Chen, Jie Tsakmaklis, Nickolas Kanan, Sandra Castillo, Jorge J Treon, Steven P Producer: 20150410 In: British journal of haematology vol. 168 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4636.	DICER1 mutations in a patient with an ovarian Sertoli-Leydig tumor, well-differentiated fetal adenocarcinoma of the lung, and familial multinodular goiter. [electronic resource] by Wu, Yingchen Chen, Dongmei Li, Yangzhi Bian, Lijuan Ma, Tingting Xie, Meiqing Producer: 20150724 In: European journal of medical genetics vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4637.	Autosomal recessive GJA1 (Cx43) gene mutations cause oculodentodigital dysplasia by distinct mechanisms. [electronic resource] by Huang, Tao Shao, Qing MacDonald, Andrew Xin, Li Lorentz, Robert Bai, Donglin Laird, Dale W Producer: 20140116 In: Journal of cell science vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4638.	Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case series. [electronic resource] by Partemi, Sara Vidal, Monica Coll Striano, Pasquale Campuzano, Oscar Allegue, Catarina Pezzella, Marianna Elia, Maurizio Parisi, Pasquale Belcastro, Vincenzo Casellato, Susanna Giordano, Lucio Mastrangelo, Massimo Pietrafusa, Nicola Striano, Salvatore Zara, Federico Bianchi, Amedeo Buti, Daniela La Neve, Angela Tassinari, Carlo Alberto Oliva, Antonio Brugada, Ramon Producer: 20160205 In: International journal of legal medicine vol. 129 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4639.	Discovery and refinement of muscle weight QTLs in B6 × D2 advanced intercross mice. [electronic resource] by Carbonetto, P Cheng, R Gyekis, J P Parker, C C Blizard, D A Palmer, A A Lionikas, A Producer: 20151026 In: Physiological genomics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4640.	Clinical and molecular findings in three Moroccan families with distal renal tubular acidosis and deafness: Report of a novel mutation of ATP6V1B1 gene. [electronic resource] by Boualla, L Jdioui, W Soulami, K Ratbi, I Sefiani, A Producer: 20180405 In: Current research in translational medicine vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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