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	1.	Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: Clinical and molecular characterization of a new contiguous gene syndrome. [electronic resource] by Souza, Josiane Faucz, Fábio Sotomaior, Vanessa Filho, Aguinaldo Bonalumi Rosenfeld, Jill Raskin, Salmo Producer: 20120823 In: Genetics and molecular biology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Somatic/gonadal mosaicism in a syndromic form of ectrodactyly, including eye abnormalities, documented through array-based comparative genomic hybridization. [electronic resource] by Filho, Aguinaldo Bonalumi Souza, Josiane Faucz, Fábio Rueda Sotomaior, Vanessa Santos Dupont, Barbara Bartel, Frank Rodriguez, Reycel Schwartz, Charles E Skinner, Cindy Alliman, Sarah Raskin, Salmo 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)

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