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	1821.	Congenital minor anomalies in mentally retarded children. [electronic resource] by Arima, M Komiya, K Ono, K Hisada, K Producer: 19690401 In: Proceedings of the Australian Association of Neurologists vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	1822.	Mice with defects in HB-EGF ectodomain shedding show severe developmental abnormalities. [electronic resource] by Yamazaki, Satoru Iwamoto, Ryo Saeki, Kazuko Asakura, Masanori Takashima, Seiji Yamazaki, Ayano Kimura, Rina Mizushima, Hiroto Moribe, Hiroki Higashiyama, Shigeki Endoh, Masayuki Kaneda, Yasufumi Takagi, Satoshi Itami, Satoshi Takeda, Naoki Yamada, Gen Mekada, Eisuke Producer: 20040112 In: The Journal of cell biology vol. 163 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1823.	Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome. [electronic resource] by Schulz, A L Albrecht, B Arici, C van der Burgt, I Buske, A Gillessen-Kaesbach, G Heller, R Horn, D Hübner, C A Korenke, G C König, R Kress, W Krüger, G Meinecke, P Mücke, J Plecko, B Rossier, E Schinzel, A Schulze, A Seemanova, E Seidel, H Spranger, S Tuysuz, B Uhrig, S Wieczorek, D Kutsche, K Zenker, M Producer: 20080229 In: Clinical genetics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1824.	Evaluating the effectiveness of psychosocial interventions for individuals with visible differences: a systematic review of the empirical literature. [electronic resource] by Bessell, Alyson Moss, Timothy P Producer: 20080129 In: Body image vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1825.	The value of sacral skin lesions in predicting occult spinal dysraphism in children with voiding dysfunction and normal neurological examination. [electronic resource] by Tarcan, Tufan Tinay, Ilker Temiz, Yusuf Alpay, Harika Ozek, Memet Simsek, Ferruh Producer: 20120628 In: Journal of pediatric urology vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1826.	Molecular and clinical characterization of cardio-facio-cutaneous (CFC) syndrome: overlapping clinical manifestations with Costello syndrome. [electronic resource] by Narumi, Yoko Aoki, Yoko Niihori, Tetsuya Neri, Giovanni Cavé, Hélène Verloes, Alain Nava, Caroline Kavamura, Maria Ines Okamoto, Nobuhiko Kurosawa, Kenji Hennekam, Raoul C M Wilson, Louise C Gillessen-Kaesbach, Gabriele Wieczorek, Dagmar Lapunzina, Pablo Ohashi, Hirofumi Makita, Yoshio Kondo, Ikuko Tsuchiya, Shigeru Ito, Etsuro Sameshima, Kiyoko Kato, Kumi Kure, Shigeo Matsubara, Yoichi Producer: 20070516 In: American journal of medical genetics. Part A vol. 143A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1827.	Clinical features and respiratory complications in Myhre syndrome. [electronic resource] by McGowan, Ruth Gulati, Ramkumar McHenry, Pamela Cooke, Alexander Butler, Sandra Keng, Wee Teik Murday, Victoria Whiteford, Margo Dikkers, Frederik G Sikkema-Raddatz, Brigit van Essen, Ton Tolmie, John Producer: 20120111 In: European journal of medical genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1828.	Clinical benefit of cetuximab and prognostic value of cetuximab-related skin toxicity in metastatic colorectal cancer: a single institution analysis. [electronic resource] by Cvetanovic, Ana Vrbic, Svetislav Filipovic, Sladjana Pejcic, Ivica Milenkovic, Dusan Zivkovic, Nikola Kostic, Milos Petkovic, Ivan Producer: 20140515 In: Journal of B.U.ON. : official journal of the Balkan Union of Oncology vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	1829.	Which chromosomal syndromes can be managed medically. [electronic resource] by de Grouchy, J Producer: 19800417 In: Progress in clinical and biological research vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	1830.	[Hydrotic (minor) form of ectodermal dysplasia]. [electronic resource] by Dethlefs, B Tronnier, H Producer: 19730323 In: Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	1831.	Prenatal diagnosis for recessive dystrophic epidermolysis bullosa in 10 families by mutation and haplotype analysis in the type VII collagen gene (COL7A1). [electronic resource] by Christiano, A M LaForgia, S Paller, A S McGuire, J Shimizu, H Uitto, J Producer: 19970102 In: Molecular medicine (Cambridge, Mass.) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	1832.	Normalization of hair growth in sparse fur-abnormal skin and hair (SPF-ASH) mice by introduction of the rat ornithine transcarbamylase (OTC) gene. [electronic resource] by Shimada, T Tashiro, M Kanzaki, T Noda, T Murakami, T Takiguchi, M Mori, M Yamamura, K Saheki, T Producer: 19950124 In: Journal of dermatological science vol. 7 Suppl Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1833.	Mutations in RIPK4 cause the autosomal-recessive form of popliteal pterygium syndrome. [electronic resource] by Kalay, Ersan Sezgin, Orhan Chellappa, Vasant Mutlu, Mehmet Morsy, Heba Kayserili, Hulya Kreiger, Elmar Cansu, Aysegul Toraman, Bayram Abdalla, Ebtesam Mohammed Aslan, Yakup Pillai, Shiv Akarsu, Nurten A Producer: 20120312 In: American journal of human genetics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1834.	The mouse waved-2 phenotype results from a point mutation in the EGF receptor tyrosine kinase. [electronic resource] by Luetteke, N C Phillips, H K Qiu, T H Copeland, N G Earp, H S Jenkins, N A Lee, D C Producer: 19940408 In: Genes & development vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1835.	IKK1-deficient mice exhibit abnormal development of skin and skeleton. [electronic resource] by Li, Q Lu, Q Hwang, J Y Büscher, D Lee, K F Izpisua-Belmonte, J C Verma, I M Producer: 19990624 In: Genes & development vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1836.	[Cutaneous nodules in neonates]. [electronic resource] by Bodemer, C Fraitag, S Producer: 20000317 In: Annales de dermatologie et de venereologie vol. 126 Availability: No items available. Save to lists Add to cart (remove)
	1837.	Congenital defects in newborn foals of mares treated for equine protozoal myeloencephalitis during pregnancy. [electronic resource] by Toribio, R E Bain, F T Mrad, D R Messer, N T Sellers, R S Hinchcliff, K W Producer: 19980423 In: Journal of the American Veterinary Medical Association vol. 212 Availability: No items available. Save to lists Add to cart (remove)
	1838.	Scd1ab-Xyk: a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse. [electronic resource] by Lu, Y Bu, L Zhou, S Jin, M Sundberg, J P Jiang, H Qian, M Shi, Y Zhao, G Kong, X Hu, L Producer: 20050322 In: Molecular genetics and genomics : MGG vol. 272 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1839.	Genetic analysis of the FOXL2 gene using quantitative real-time PCR in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome. [electronic resource] by Hu, Shanshan Guo, Junjing Wang, Binbin Wang, Jing Zhou, Zhou Zhou, Guangkai Ding, Xuchen Ma, Xu Qi, Yanhua Producer: 20110526 In: Molecular vision vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	1840.	Arteriolar Hyalinosis Predicts Increase in Albuminuria and GFR Decline in Normo- and Microalbuminuric Japanese Patients With Type 2 Diabetes. [electronic resource] by Moriya, Tatsumi Omura, Kazuki Matsubara, Madoka Yoshida, Yuki Hayama, Kei Ouchi, Motoshi Producer: 20180320 In: Diabetes care vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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