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	1.	Transcriptomic analysis of FUCA1 knock-down in keratinocytes reveals new insights into the pathogenesis of fucosidosis skin lesions. [electronic resource] by Valero-Rubio, Danyela Jiménez, Karen Marcela Fonseca, Dora Janeth Payán-Gómez, César Laissue, Paul Producer: 20190520 In: Experimental dermatology vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Sequence analysis of the ADRA2A coding region in children affected by attention deficit hyperactivity disorder. [electronic resource] by Castro, Taryn Mateus, Heidi Eliana Fonseca, Dora Janeth Forero, Diego Restrepo, Carlos Martín Talero, Claudia Vélez, Alberto Laissue, Paul Producer: 20140723 In: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Screening for mutations of the FOXO4 gene in premature ovarian failure patients. [electronic resource] by Fonseca, Dora Janeth Garzón, Eliana Lakhal, Besma Braham, Rim Ojeda, Diego Elghezal, Hatem Saâd, Ali Restrepo, Carlos Martín Laissue, Paul Producer: 20121130 In: Reproductive biomedicine online vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	THBD sequence variants potentially related to recurrent pregnancy loss. [electronic resource] by Quintero-Ronderos, Paula Mercier, Eric Gris, Jean-Christophe Esteban-Perez, Clara Moreno-Ortiz, Harold Fonseca, Dora Janeth Lucena, Elkin Vaiman, Daniel Laissue, Paul Producer: 20180808 In: Reproductive biology and endocrinology : RB&E vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A de novo 14q12q13.3 interstitial deletion in a patient affected by a severe neurodevelopmental disorder of unknown origin. [electronic resource] by Fonseca, Dora Janeth Prada, Carlos Fernando Siza, Luz Miriam Angel, Diana Gomez, Yenny Milena Restrepo, Carlos Martin Douben, Hannie Rivadeneira, Fernando de Klein, Annelies Laissue, Paul Producer: 20120604 In: American journal of medical genetics. Part A vol. 158A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Next generation sequencing in women affected by nonsyndromic premature ovarian failure displays new potential causative genes and mutations. [electronic resource] by Fonseca, Dora Janeth Patiño, Liliana Catherine Suárez, Yohjana Carolina de Jesús Rodríguez, Asid Mateus, Heidi Eliana Jiménez, Karen Marcela Ortega-Recalde, Oscar Díaz-Yamal, Ivonne Laissue, Paul Producer: 20150921 In: Fertility and sterility vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Identification and Functional Characterization of GAA Mutations in Colombian Patients Affected by Pompe Disease. [electronic resource] by Niño, Mónica Yasmín Mateus, Heidi Eliana Fonseca, Dora Janeth Kroos, Marian A Ospina, Sandra Yaneth Mejía, Juan Fernando Uribe, Jesús Alfredo Reuser, Arnold J J Laissue, Paul Producer: 20130225 In: JIMD reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Creating and validating a warfarin pharmacogenetic dosing algorithm for Colombian patients. [electronic resource] by Galvez, Jubby Marcela Restrepo, Carlos Martin Contreras, Nora Constanza Alvarado, Clara Calderón-Ospina, Carlos-Alberto Peña, Nidia Cifuentes, Ricardo A Duarte, Daniela Laissue, Paul Fonseca, Dora Janeth Publication details: Pharmacogenomics and personalized medicine 2018 In: Pharmacogenomics and personalized medicine vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A novel familial case of diffuse leukodystrophy related to NDUFV1 compound heterozygous mutations. [electronic resource] by Ortega-Recalde, Oscar Fonseca, Dora Janeth Patiño, Liliana Catherine Atuesta, Juan Jaime Rivera-Nieto, Carolina Restrepo, Carlos Martín Mateus, Heidi Eliana van der Knaap, Marjo S Laissue, Paul Producer: 20140715 In: Mitochondrion vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	BMP15 c.-9C>G promoter sequence variant may contribute to the cause of non-syndromic premature ovarian failure. [electronic resource] by Fonseca, Dora Janeth Ortega-Recalde, Oscar Esteban-Perez, Clara Moreno-Ortiz, Harold Patiño, Liliana Catherine Bermúdez, Olga María Ortiz, Angela María Restrepo, Carlos M Lucena, Elkin Laissue, Paul Producer: 20150812 In: Reproductive biomedicine online vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Whole-exome sequencing enables rapid determination of xeroderma pigmentosum molecular etiology. [electronic resource] by Ortega-Recalde, Oscar Vergara, Jéssica Inés Fonseca, Dora Janeth Ríos, Xiomara Mosquera, Hernando Bermúdez, Olga María Medina, Claudia Liliana Vargas, Clara Inés Pallares, Argemiro Enrique Restrepo, Carlos Martín Laissue, Paul Producer: 20150128 In: PloS one vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia. [electronic resource] by Quintero-Ronderos, Paula Jiménez, Karen Marcela Esteban-Pérez, Clara Ojeda, Diego A Bello, Sandra Fonseca, Dora Janeth Coronel, María Alejandra Moreno-Ortiz, Harold Sierra-Díaz, Diana Carolina Lucena, Elkin Barbaux, Sandrine Vaiman, Daniel Laissue, Paul Producer: 20200706 In: Molecular medicine (Cambridge, Mass.) vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	CITED2 mutations potentially cause idiopathic premature ovarian failure. [electronic resource] by Fonseca, Dora Janeth Ojeda, Diego Lakhal, Besma Braham, Rim Eggers, Stefanie Turbitt, Erin White, Stefan Grover, Sonia Warne, Garry Zacharin, Margaret Nevin Lam, Alexandra Landolsi, Hanène Elghezal, Hatem Saâd, Ali Restrepo, Carlos Martín Fellous, Marc Sinclair, Andrew Koopman, Peter Laissue, Paul Producer: 20130306 In: Translational research : the journal of laboratory and clinical medicine vol. 160 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)