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	1.	Comparing the Sexual Reproductive Success of Two Exotic Trees Invading Spanish Riparian Forests vs. a Native Reference. [electronic resource] by Cabra-Rivas, Isabel Castro-Díez, Pilar Producer: 20170731 In: PloS one vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Targeting to macrophages: role of physicochemical properties of particulate carriers--liposomes and microspheres--on the phagocytosis by macrophages. [electronic resource] by Ahsan, Fakhrul Rivas, Isabel P Khan, Mansoor A Torres Suarez, Ana I Producer: 20020516 In: Journal of controlled release : official journal of the Controlled Release Society vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Ovarian maldescent. [electronic resource] by Trinidad, Carmen Tardáguila, Francisco Fernández, Gabriel C Martínez, Concepción Chávarri, Elena Rivas, Isabel Producer: 20041102 In: European radiology vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	[CHARGE syndrome]. [electronic resource] by Lobete Prieto, Carlos Javier Llano Rivas, Isabel Fernández Toral, Joaquín Madero Barrajón, Pilar Producer: 20100630 In: Archivos argentinos de pediatria vol. 108 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A novel mutation in the IRF6 gene associated with facial asymmetry in a family affected with Van der Woude syndrome. [electronic resource] by Miñones-Suárez, Lorena Mas-Vidal, Alberto Fernandez-Toral, Joaquin Llano-Rivas, Isabel González-García, Manuel Producer: 20130909 In: Pediatric dermatology vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	In-frame deletion in FLNA causing familial periventricular heterotopia with skeletal dysplasia in males. [electronic resource] by Parrini, Elena Rivas, Isabel Llano Toral, Joaquin Fernandez Pucatti, Daniela Giglio, Sabrina Mei, Davide Guerrini, Renzo Producer: 20110801 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)
	7.	Delineation of the clinically recognizable 17q22 contiguous gene deletion syndrome in a patient carrying the smallest microdeletion known to date. [electronic resource] by Martínez-Fernández, María Luisa Fernández-Toral, Joaquin Llano-Rivas, Isabel Bermejo-Sánchez, Eva MacDonald, Alexandra Martínez-Frías, María Luisa Producer: 20160519 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)
	8.	Endovascular treatment of iliofemoral chronic post-thrombotic venous flow obstruction. [electronic resource] by Blanch Alerany, Montserrat Izquierdo Lamoca, Luis Miguel Ramirez Ortega, Marta Lago Rivas, Isabel Zotta Desboeufs, Romina Stefanov Kiuri, Stefan Producer: 20160323 In: Journal of vascular surgery. Venous and lymphatic disorders vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Cri-du-chat syndrome mimics Silver-Russell syndrome depending on the size of the deletion: a case report. [electronic resource] by Vado, Yerai Errea-Dorronsoro, Javier Llano-Rivas, Isabel Gorria, Nerea Pereda, Arrate Gener, Blanca Garcia-Naveda, Laura Perez de Nanclares, Guiomar Producer: 20190725 In: BMC medical genomics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Interaction between a Domain of the Negative Regulator of the Ras-ERK Pathway, SPRED1 Protein, and the GTPase-activating Protein-related Domain of Neurofibromin Is Implicated in Legius Syndrome and Neurofibromatosis Type 1. [electronic resource] by Hirata, Yasuko Brems, Hilde Suzuki, Mayu Kanamori, Mitsuhiro Okada, Masahiro Morita, Rimpei Llano-Rivas, Isabel Ose, Toyoyuki Messiaen, Ludwine Legius, Eric Yoshimura, Akihiko Producer: 20160706 In: The Journal of biological chemistry vol. 291 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Clinical and genetic findings in five female patients with haemophilia A: Identification of a novel missense mutation, p.Phe2127Ser. [electronic resource] by Martín-Salces, Mónica Venceslá, Adoración Alvárez-Román, María Teresa Rivas, Isabel Fernandez, Ihosvany Butta, Nora Baena, Manel Fuentes-Prior, Pablo Tizzano, Eduardo F Jiménez-Yuste, Víctor Producer: 20110511 In: Thrombosis and haemostasis vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Exome sequencing identifies CTSK mutations in patients originally diagnosed as intermediate osteopetrosis. [electronic resource] by Pangrazio, Alessandra Puddu, Alessandro Oppo, Manuela Valentini, Maria Zammataro, Luca Vellodi, Ashok Gener, Blanca Llano-Rivas, Isabel Raza, Jamal Atta, Irum Vezzoni, Paolo Superti-Furga, Andrea Villa, Anna Sobacchi, Cristina Producer: 20140909 In: Bone vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Association of DRD2 variants and Gilles de la Tourette syndrome in a family-based sample from a South American population isolate. [electronic resource] by Herzberg, Ibi Valencia-Duarte, Ana Victoria Kay, Victoria A White, Daniel J Müller, Heike Rivas, Isabel C Mesa, Sandra Catalina Cuartas, Mauricio García, Jharley Bedoya, Gabriel Cornejo, William Ruiz-Linares, Andrés Kremeyer, Barbara Producer: 20101104 In: Psychiatric genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	A kidney-disease gene panel allows a comprehensive genetic diagnosis of cystic and glomerular inherited kidney diseases. [electronic resource] by Bullich, Gemma Domingo-Gallego, Andrea Vargas, Iván Ruiz, Patricia Lorente-Grandoso, Laura Furlano, Mónica Fraga, Gloria Madrid, Álvaro Ariceta, Gema Borregán, Mar Piñero-Fernández, Juan Alberto Rodríguez-Peña, Lidia Ballesta-Martínez, Maria Juliana Llano-Rivas, Isabel Meñica, Mireia Aguirre Ballarín, José Torrents, David Torra, Roser Ars, Elisabet Producer: 20190528 In: Kidney international vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing. [electronic resource] by Calmels, Nadège Greff, Géraldine Obringer, Cathy Kempf, Nadine Gasnier, Claire Tarabeux, Julien Miguet, Marguerite Baujat, Geneviève Bessis, Didier Bretones, Patricia Cavau, Anne Digeon, Béatrice Doco-Fenzy, Martine Doray, Bérénice Feillet, François Gardeazabal, Jesus Gener, Blanca Julia, Sophie Llano-Rivas, Isabel Mazur, Artur Michot, Caroline Renaldo-Robin, Florence Rossi, Massimiliano Sabouraud, Pascal Keren, Boris Depienne, Christel Muller, Jean Mandel, Jean-Louis Laugel, Vincent Producer: 20160930 In: Orphanet journal of rare diseases vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1. [electronic resource] by Nag, Abhishek Bochukova, Elena G Kremeyer, Barbara Campbell, Desmond D Muller, Heike Valencia-Duarte, Ana V Cardona, Julio Rivas, Isabel C Mesa, Sandra C Cuartas, Mauricio Garcia, Jharley Bedoya, Gabriel Cornejo, William Herrera, Luis D Romero, Roxana Fournier, Eduardo Reus, Victor I Lowe, Thomas L Farooqi, I Sadaf Mathews, Carol A McGrath, Lauren M Yu, Dongmei Cook, Ed Wang, Kai Scharf, Jeremiah M Pauls, David L Freimer, Nelson B Plagnol, Vincent Ruiz-Linares, Andrés Producer: 20130911 In: PloS one vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment. [electronic resource] by Salpietro, Vincenzo Malintan, Nancy T Llano-Rivas, Isabel Spaeth, Christine G Efthymiou, Stephanie Striano, Pasquale Vandrovcova, Jana Cutrupi, Maria C Chimenz, Roberto David, Emanuele Di Rosa, Gabriella Marce-Grau, Anna Raspall-Chaure, Miquel Martin-Hernandez, Elena Zara, Federico Minetti, Carlo Bello, Oscar D De Zorzi, Rita Fortuna, Sara Dauber, Andrew Alkhawaja, Mariam Sultan, Tipu Mankad, Kshitij Vitobello, Antonio Thomas, Quentin Mau-Them, Frederic Tran Faivre, Laurence Martinez-Azorin, Francisco Prada, Carlos E Macaya, Alfons Kullmann, Dimitri M Rothman, James E Krishnakumar, Shyam S Houlden, Henry Producer: 20200203 In: American journal of human genetics vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Clinical and Molecular Description of 16 Families With Heterozygous IHH Variants. [electronic resource] by Sentchordi-Montané, Lucía Benito-Sanz, Sara Aza-Carmona, Miriam Pereda, Arrate Parrón-Pajares, Manuel de la Torre, Carolina Vasques, Gabriela A Funari, Mariana F A Travessa, André M Dias, Patrícia Suarez-Ortega, Larisa González-Buitrago, Jesús Portillo-Najera, Nancy Elizabeth Llano-Rivas, Isabel Martín-Frías, María Ramírez-Fernández, Joaquín Sánchez Del Pozo, Jaime Garzón-Lorenzo, Lucía Martos-Moreno, Gabriel A Alfaro-Iznaola, Cristina Mulero-Collantes, Inés Ruiz-Ocaña, Pablo Casano-Sancho, Paula Portela, Ana Ruiz-Pérez, Lorea Del Pozo, Angela Vallespín, Elena Solís, Mario Lerario, Antônio M González-Casado, Isabel Ros-Pérez, Purificación Pérez de Nanclares, Guiomar Jorge, Alexander A L Heath, Karen E Producer: 20210208 In: The Journal of clinical endocrinology and metabolism vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype Correlation. [electronic resource] by Rojnueangnit, Kitiwan Xie, Jing Gomes, Alicia Sharp, Angela Callens, Tom Chen, Yunjia Liu, Ying Cochran, Meagan Abbott, Mary-Alice Atkin, Joan Babovic-Vuksanovic, Dusica Barnett, Christopher P Crenshaw, Melissa Bartholomew, Dennis W Basel, Lina Bellus, Gary Ben-Shachar, Shay Bialer, Martin G Bick, David Blumberg, Bruce Cortes, Fanny David, Karen L Destree, Anne Duat-Rodriguez, Anna Earl, Dawn Escobar, Luis Eswara, Marthanda Ezquieta, Begona Frayling, Ian M Frydman, Moshe Gardner, Kathy Gripp, Karen W Hernández-Chico, Concepcion Heyrman, Kurt Ibrahim, Jennifer Janssens, Sandra Keena, Beth A Llano-Rivas, Isabel Leppig, Kathy McDonald, Marie Misra, Vinod K Mulbury, Jennifer Narayanan, Vinodh Orenstein, Naama Galvin-Parton, Patricia Pedro, Helio Pivnick, Eniko K Powell, Cynthia M Randolph, Linda Raskin, Salmo Rosell, Jordi Rubin, Karol Seashore, Margretta Schaaf, Christian P Scheuerle, Angela Schultz, Meredith Schorry, Elizabeth Schnur, Rhonda Siqveland, Elizabeth Tkachuk, Amanda Tonsgard, James Upadhyaya, Meena Verma, Ishwar C Wallace, Stephanie Williams, Charles Zackai, Elaine Zonana, Jonathan Lazaro, Conxi Claes, Kathleen Korf, Bruce Martin, Yolanda Legius, Eric Messiaen, Ludwine Producer: 20160726 In: Human mutation vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy. [electronic resource] by Ochoa, Juan Pablo Sabater-Molina, María García-Pinilla, José Manuel Mogensen, Jens Restrepo-Córdoba, Alejandra Palomino-Doza, Julián Villacorta, Eduardo Martinez-Moreno, Marina Ramos-Maqueda, Javier Zorio, Esther Peña-Peña, Maria L García-Granja, Pablo E Rodríguez-Palomares, José F Cárdenas-Reyes, Ivonne J de la Torre-Carpente, María M Bautista-Pavés, Alicia Akhtar, Mohammed M Cicerchia, Marcos N Bilbao-Quesada, Raquel Mogollón-Jimenez, Maria Victoria Salazar-Mendiguchía, Joel Mesa Latorre, José M Arnaez, Blanca Olavarri-Miguel, Ivan Fuentes-Cañamero, María E Lamounier, Arsonval Pérez Ruiz, José María Climent-Payá, Vicente Pérez-Sanchez, Inmaculada Trujillo-Quintero, Juan P Lopes, Luis R Repáraz-Andrade, Alfredo Marín-Iglesias, Rosario Rodriguez-Vilela, Alejandro Sandín-Fuentes, María Garrote, Jose A Cortel-Fuster, Alejandro Lopez-Garrido, Miguel Fontalba-Romero, Ana Ripoll-Vera, Tomás Llano-Rivas, Isabel Fernandez-Fernandez, Xusto Isidoro-García, María Garcia-Giustiniani, Diego Barriales-Villa, Roberto Ortiz-Genga, Martín García-Pavía, Pablo Elliott, Perry M Gimeno, Juan R Monserrat, Lorenzo Producer: 20190912 In: Journal of the American College of Cardiology vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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