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	1.	The craniocardioskeletal syndrome and the Noonan-like short stature syndrome are possibly the same entity. [electronic resource] by Sánchez Corona, J Cantú, J M Producer: 19871110 In: Journal of medical genetics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	[Teratogenic effect of metronidazole on the prosencephalon]. [electronic resource] by Sánchez-Corona, J García-Cruz, D Cantú, J M Producer: 19831021 In: Gaceta medica de Mexico vol. 119 Availability: No items available. Save to lists Add to cart (remove)
	3.	Osteopoikilosis: report of a familial case. [electronic resource] by Sarralde, A Garcia-Cruz, D Nazara, Z Sanchez-Corona, J Producer: 19950420 In: Genetic counseling (Geneva, Switzerland) vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	4.	Omphalocele-exstrophy-imperforate-anus-spina bifida (OEIS) complex in a male prenatally exposed to diazepam. [electronic resource] by Lizcano-Gil, L A García-Cruz, D Sánchez-Corona, J Producer: 19950516 In: Archives of medical research vol. 26 Availability: No items available. Save to lists Add to cart (remove)
	5.	De novo t(4;5)(q3100;q2200) with del(5)(q1500q2200). Tentative delineation of a 5q monosomy syndrome and assignment of the critical segment. [electronic resource] by Rivera, H Rolón, A Sánchez-Corona, J Cantú, J M Producer: 19850426 In: Clinical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	[Qualitative and quantitative determination of urinary glycosaminoglycans in patients with osteochondrodysplasias]. [electronic resource] by Sánchez-Corona, J Gallegos-Arreola, M P Contreras-Sánchez, O Producer: 19931027 In: Archivos de investigacion medica vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	7.	[Acid hydrolysis of urinary oligosaccharides in type I glycogenosis]. [electronic resource] by Sánchez-Corona, J Mora-García, H A Contreras-Sánchez, O Producer: 19931027 In: Archivos de investigacion medica vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	8.	Dominant inheritance of holoprosencephaly. [electronic resource] by Cantú, J M Fragoso, R Garcia-Cruz, D Sánchez-Corona, J Producer: 19790324 In: Birth defects original article series vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	9.	Severe mental deficiency, proportionate dwarfism, and delayed sexual maturation. A distinct inherited syndrome. [electronic resource] by Cantú, J M Sánchez-Corona, J García-Cruz, D Fragoso, R Producer: 19810327 In: Human genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	A distinct dominant form of microtia and conductive hearing loss. [electronic resource] by Sánchez-Corona, J García-Cruz, D Ruenes, R Cantú, J M Producer: 19830127 In: Birth defects original article series vol. 18 Availability: No items available. Save to lists Add to cart (remove)
	11.	De novo duplication xq22-q23 in a girl with short stature and gonadal dysgenesis. [electronic resource] by Correa-Cerro, L Garcia-Cruz, D Ruiz, M X Sanchez-Corona, J Producer: 19990518 In: Annales de genetique vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	12.	A simple screening procedure for adenylate kinase, hexokinase and glucose-6-phosphate dehydrogenase deficiencies. [electronic resource] by Vaca, G Sanchez-Corona, J Olivares, N Medina, C Cantu, J M Producer: 19801218 In: Annales de genetique vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	13.	A distinct osteochondrodysplasia with hypertrichosis- Individualization of a probable autosomal recessive entity. [electronic resource] by Cantú, J M García-Cruz, D Sánchez-Corona, J Hernández, A Nazará, Z Producer: 19820719 In: Human genetics vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Partial trisomy 1q and monosomy 18q due to a de novo t(1;18)(q25;q23). [electronic resource] by Solé, M T Rivera, H Sánchez-Corona, J Plascencia, L Cantú, J M Producer: 19831008 In: Annales de genetique vol. 26 Availability: No items available. Save to lists Add to cart (remove)
	15.	Individualization of a syndrome with mental deficiency, macrocranium, peculiar facies, and cardiac and skeletal anomalies. [electronic resource] by Cantú, J M Sánchez-Corona, J Hernándes, A Nazará, Z García-Cruz, D Producer: 19830317 In: Clinical genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Spondylo-camptodactyly syndrome: a distinct autosomal dominant entity? [electronic resource] by Lizcano-Gil, L A García-Cruz, D Sánchez-Corona, J Cantú, J M Producer: 19960401 In: Clinical genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	An extra idic(21)(q22.1) in a child with some features of Down's syndrome. [electronic resource] by Gütiérrez-Angulo, M Ramos, A L Dávalos, N Sánchez-Corona, J Rivera, H Producer: 19990618 In: Clinical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Familial comedones. Evidence for autosomal dominant inheritance. [electronic resource] by Cantú, J M Gómez-Bustamente, M O González-Mendoza, A Sánchez-Corona, J Producer: 19790324 In: Archives of dermatology vol. 114 Availability: No items available. Save to lists Add to cart (remove)
	19.	Partial mispairing and crossing-over between beta 0 and delta genes as the origin of the delta beta 0 thalassemia gene. A single mutational event hypothesis. [electronic resource] by Cantú, J M Ibarra, B Vaca, G Ramirez, M L Sánchez-Corona, J Producer: 19791024 In: Human genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Deletion of 7q22 and ectrodactyly. [electronic resource] by Rivera, H Sanchez-Corona, J Burgos-Fuentes, V R Melendez-Ruiz, M J Producer: 19920113 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 110 results.