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	1.	An update on amniotic bands sequence. [electronic resource] by López-Muñoz, Eunice Becerra-Solano, Luis E Producer: 20190828 In: Archivos argentinos de pediatria vol. 116 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	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)
	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.	First case reported of Turner syndrome and trisomy 14 chromosomal mosaicism in a patient. [electronic resource] by Becerra-Solano, Luis E Arnaud-Lopez, Lisette Diaz-Rodriguez, Manuel Mantilla-Capacho, Johana M Nastasi-Catanese, Jose A Ortiz-Aranda, Martha Vasquez, Ana I Figuera, Luis E Producer: 20080429 In: Clinical dysmorphology vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	The fifth female patient with Myhre syndrome: further delineation. [electronic resource] by Becerra-Solano, Luis E Díaz-Rodriguez, Manuel Nastasi-Catanese, Jose A Toscano-Flores, Jose J Bañuelos-Robles, Oscar Figuera, Luis E Matute, Esmeralda de Lourdes Ramírez-Dueñas, Maria Producer: 20080527 In: Clinical dysmorphology vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	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)
	7.	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)