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	1.	Expanding the phenotype of spondylospinal thoracic dysostosis (the Turkel-Chen-Johnson syndrome). [electronic resource] by Becerra-Solano, Luis E Chacon, Liliana Morales-Mata, Dinorah Ramírez-Dueñas, Maria de Lourdes García-Ortiz, José E Producer: 20150721 In: Clinical dysmorphology vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Split hand malformation, hypospadias, microphthalmia, distinctive face and short stature in two brothers suggest a new syndrome. [electronic resource] by García-Ortiz, Jose E Banda-Espinoza, Felipe Zenteno, Juan C Galván-Uriarte, Luz M Ruiz-Flores, Pablo García-Cruz, Diana Producer: 20050531 In: American journal of medical genetics. Part A vol. 135 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Bosma arrhinia microphthalmia syndrome in a Mexican patient with a molecular analysis of PAX6. [electronic resource] by Becerra-Solano, Luis E Chacón, Liliana Morales-Mata, Dinorah Zenteno, Juan C Ramírez-Dueñas, Maria L García-Ortiz, Jose E Producer: 20160928 In: Clinical dysmorphology vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	[Anterior cervical hypertrichosis: case report]. [electronic resource] by Orozco-Gutiérrez, Mario H Sánchez-Corona, José García-Ortiz, José E Castañeda-Cisneros, Gema Dávalos-Rodríguez, Nory O Corona-Rivera, Jorge R García-Cruz, Diana Producer: 20180129 In: Archivos argentinos de pediatria vol. 114 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Alopecia Areata. Current situation and perspectives. [electronic resource] by Juárez-Rendón, Karina J Rivera Sánchez, Gildardo Reyes-López, Miguel Á García-Ortiz, José E Bocanegra-García, Virgilio Guardiola-Avila, Iliana Altamirano-García, María L Producer: 20180716 In: Archivos argentinos de pediatria vol. 115 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Two girls with a de novo Xq rearrangement of paternal origin: t(X;9)(q24;q12) or rea(X)dup q. [electronic resource] by Vásquez-Velásquez, Ana I Rivera, Horacio Castro, Ana G Jaloma-Cruz, Ana R Juárez, Clara I Lara-Navarro, Irving J Córdova-Fletes, Carlos Mendoza-Pérez, Paul García-Ortiz, José E Producer: 20170425 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)
	7.	Uncommon runs of homozygosity disclose homozygous missense mutations in two ciliopathy-related genes (SPAG17 and WDR35) in a patient with multiple brain and skeletal anomalies. [electronic resource] by Córdova-Fletes, Carlos Becerra-Solano, Luis E Rangel-Sosa, Martha M Rivas-Estilla, Ana María Alberto Galán-Huerta, Kame Ortiz-López, Rocío Rojas-Martínez, Augusto Juárez-Vázquez, Clara I García-Ortiz, José E Producer: 20180918 In: European journal of medical genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder. [electronic resource] by García-Ortiz, José E Zarazúa-Niño, Ana I Hernández-Orozco, Angélica A Reyes-Oliva, Edwin A Pérez-Ávila, Carlos E Becerra-Solano, Luis E Galán-Huerta, Kame A Rivas-Estilla, Ana M Córdova-Fletes, Carlos Publication details: Journal of autism and developmental disorders 06 2020 In: Journal of autism and developmental disorders vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome. [electronic resource] by Shaw, Natalie D Brand, Harrison Kupchinsky, Zachary A Bengani, Hemant Plummer, Lacey Jones, Takako I Erdin, Serkan Williamson, Kathleen A Rainger, Joe Stortchevoi, Alexei Samocha, Kaitlin Currall, Benjamin B Dunican, Donncha S Collins, Ryan L Willer, Jason R Lek, Angela Lek, Monkol Nassan, Malik Pereira, Shahrin Kammin, Tammy Lucente, Diane Silva, Alexandra Seabra, Catarina M Chiang, Colby An, Yu Ansari, Morad Rainger, Jacqueline K Joss, Shelagh Smith, Jill Clayton Lippincott, Margaret F Singh, Sylvia S Patel, Nirav Jing, Jenny W Law, Jennifer R Ferraro, Nalton Verloes, Alain Rauch, Anita Steindl, Katharina Zweier, Markus Scheer, Ianina Sato, Daisuke Okamoto, Nobuhiko Jacobsen, Christina Tryggestad, Jeanie Chernausek, Steven Schimmenti, Lisa A Brasseur, Benjamin Cesaretti, Claudia García-Ortiz, Jose E Buitrago, Tatiana Pineda Silva, Orlando Perez Hoffman, Jodi D Mühlbauer, Wolfgang Ruprecht, Klaus W Loeys, Bart L Shino, Masato Kaindl, Angela M Cho, Chie-Hee Morton, Cynthia C Meehan, Richard R van Heyningen, Veronica Liao, Eric C Balasubramanian, Ravikumar Hall, Janet E Seminara, Stephanie B Macarthur, Daniel Moore, Steven A Yoshiura, Koh-Ichiro Gusella, James F Marsh, Joseph A Graham, John M Lin, Angela E Katsanis, Nicholas Jones, Peter L Crowley, William F Davis, Erica E FitzPatrick, David R Talkowski, Michael E Publication details: Nature genetics 05 2017 In: Nature genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome. [electronic resource] by Shaw, Natalie D Brand, Harrison Kupchinsky, Zachary A Bengani, Hemant Plummer, Lacey Jones, Takako I Erdin, Serkan Williamson, Kathleen A Rainger, Joe Stortchevoi, Alexei Samocha, Kaitlin Currall, Benjamin B Dunican, Donncha S Collins, Ryan L Willer, Jason R Lek, Angela Lek, Monkol Nassan, Malik Pereira, Shahrin Kammin, Tammy Lucente, Diane Silva, Alexandra Seabra, Catarina M Chiang, Colby An, Yu Ansari, Morad Rainger, Jacqueline K Joss, Shelagh Smith, Jill Clayton Lippincott, Margaret F Singh, Sylvia S Patel, Nirav Jing, Jenny W Law, Jennifer R Ferraro, Nalton Verloes, Alain Rauch, Anita Steindl, Katharina Zweier, Markus Scheer, Ianina Sato, Daisuke Okamoto, Nobuhiko Jacobsen, Christina Tryggestad, Jeanie Chernausek, Steven Schimmenti, Lisa A Brasseur, Benjamin Cesaretti, Claudia García-Ortiz, Jose E Buitrago, Tatiana Pineda Silva, Orlando Perez Hoffman, Jodi D Mühlbauer, Wolfgang Ruprecht, Klaus W Loeys, Bart L Shino, Masato Kaindl, Angela M Cho, Chie-Hee Morton, Cynthia C Meehan, Richard R van Heyningen, Veronica Liao, Eric C Balasubramanian, Ravikumar Hall, Janet E Seminara, Stephanie B Macarthur, Daniel Moore, Steven A Yoshiura, Koh-Ichiro Gusella, James F Marsh, Joseph A Graham, John M Lin, Angela E Katsanis, Nicholas Jones, Peter L Crowley, William F Davis, Erica E FitzPatrick, David R Talkowski, Michael E Producer: 20170905 In: Nature genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)