232 results on '"Sánchez-Corona J"'
Search Results
2. Tumor necrosis factor haplotype diversity in Mestizo and Native populations of Mexico
3. Association analysis of the Gln223Arg polymorphism in the human leptin receptor gene, and traits related to obesity in Mexican adolescents
4. A Missense Mutation, p.V132G, in the X-Linked Spermine Synthase Gene (SMS) Causes Snyder–Robinson Syndrome
5. Methylenetetrahydrofolate reductase C677T polymorphism and Factor V Leiden variant in Mexican women with preeclampsia/eclampsia
6. Metaphyseal chondrodysplasia, upper limb mesomelia and normal height (mesomelic dysplasia camera type): Second report in a Mexican patient
7. Camptodactyly, Joint Contractures, Facial, and Skeletal Defects:: Further Delineation of the Rozin Camptodactyly Syndrome
8. DNA polymorphism analysis of candidate genes for type 2 diabetes mellitus in a Mexican ethnic group
9. Association analysis of polymorphisms in the interleukin-4 receptor (alpha) gene with atopic asthma in patients from western Mexico
10. An extra idic(21)(q22.1) in a child with some features of Down's syndrome
11. Clinical, morphological and biochemical features in the familial articular hypermobility syndrome (FAHS): a family study
12. Distribution of IFITM3 polymorphism (dbSNP: rs12252) in mestizo populations in four states of Mexico
13. Contribution of polymorphisms in the LEP, LEPR and RETN genes on serum leptin and resistin levels in young adults from Mexico
14. Acculturation impact on some metabolic parameters of the Lacandon communities from Chiapas
15. Protective role of +294 T/C (rs2016520) polymorphism of PPARD in Mexican patients with colorectal cancer
16. Severe mental deficiency, proportionate dwarfism, and delayed sexual maturation: A distinct inherited syndrome
17. Pure monosomy and trisomy 2q24.2→q3105 due to an inv ins(7;2)(q21.2;q3105q24.2) segregating in four generations
18. Partial mispairing and crossing-over between β0 and δ genes as the origin of the δ β0 thalassemia gene: A single mutational event hypothesis
19. Red blood cell sorbitol dehydrogenase deficiency in a family with cataracts
20. A distinct osteochondrodysplasia with hypertrichosis—Individualization of a probable autosomal recessive entity
21. Los Angeles variant of galactose-1-phosphate uridyltransferase (EC 2.7.7.12) in a Mexican family
22. A distinct dysmorphic syndrome with spinocerebellar ataxia and probable autosomal recessive inheritance
23. Human papillomavirus viral load in cervical intraepithelial neoplasia as a prognostic factor in a Mexican population
24. XV-2c/KM19 haplotypes analysis of cystic fibrosis patients from western Mexico
25. Christian's spondylo-digital syndrome: second familial case
26. Clinical, morphological and biochemical features in the familial articular hypermobility syndrome (FAHS): a family study
27. Spondylo-camptodactyly syndrome: a distinct autosomal dominant entity?
28. Polymorphisms in candidate genes for type 2 diabetes mellitus in a Mexican population with metabolic syndrome findings
29. Determination of diesel genotoxicity in firebreathers by micronuclei and nuclear abnormalities in buccal mucosa
30. Induction of micronuclei in the domestic cat (Felis domesticus) peripheral blood by colchicine and cytosine-arabinoside
31. Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: Further delineation of a new genetic syndrome
32. Spontaneous micronuclei in peripheral blood erythrocytes from 35 mammalian species
33. The Myhre syndrome: report of two cases
34. Poland‐Moebius syndrome in a boy and Poland syndrome in his mother
35. Christian's spondylo-digital syndrome: second familial case.
36. Spondylo-camptodactyly syndrome: a distinct autosomal dominant entity?
37. Guadalajara camptodactyly syndrome type II.
38. A 'new' autosomal dominant genodermatosis characterized by hyperpigmented spots and palmo- plantar hyperkeratosis.
39. Monosomy 13q32.3----qter: report of two cases.
40. Partial mispairing and crossing-over between β0 and δ genes as the origin of the δ β0 thalassemia gene
41. Partial mispairing and crossing-over between β0 and δ genes as the origin of the δ β0 thalassemia gene
42. Molecular analysis of northwestern Mexican patients with cystic fibrosis: screening of 10 known mutations. Mutations in brief no. 185. Online
43. Mucopolysaccharidoses type II: enzymatic activity and quantitative and qualitative studies of urinary glycosaminoglycans in five patients
44. Constitutional duplication 11q23 de novo involving the MLL gene
45. The detection of human papillomavirus 16, 18, 35 and 58 in cervical-uterine cancer and advanced degree of squamous intraepithelial lesions in Western Mexico: clinical-molecular correlation | Detección de papilomavirus humano tipos 16, 18, 35 y 58 en cáncer cervicouterino y lesiones escamosas intraepiteliales de alto grado en el occidente de México: correlación clínico-molecular
46. Pharmacogenetics and antiepileptic drug metabolism: Implication of genetic variants in cytochromes P450,Farmacogenética y metabolismo de fármacos antiepilépticos: Implicación de variantes genéticas en citocromos P1450
47. Mucopolysaccharidoses type II: Enzymatic activity and quantitative and qualitative studies of urinary glycosaminoglycans in five patients
48. Polymorphism in codon 72 of the p53 gene and cervico-uterine cancer risk in Mexico | Polimorfismo en el codón 72 del gen p53 y riesgo de cáncer cérvico-uterino en México
49. The craniocardioskeletal syndrome and the Noonan-like short stature syndrome are possibly the same entity.
50. A FEMALE CASE OF SPINOCEREBELLAR ATAXIA TYPE 10 WITH SUICIDAL BEHAVIOR AND ENDOCRINPATHIES ASSOCIATED WITH A MASSIVE EXPANSION (ATTCT) OF THE GENE ATXN10.
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