15 results on '"Sánchez-Corona J"'
Search Results
2. Tumor necrosis factor haplotype diversity in Mestizo and Native populations of Mexico
3. A missense mutation, p.V132G, in the X-linked spermine synthase gene (SMS) causes Snyder-Robinson syndrome
4. Christian's spondylo-digital syndrome: second familial case
5. Clinical, morphological and biochemical features in the familial articular hypermobility syndrome (FAHS): a family study
6. Spondylo-camptodactyly syndrome: a distinct autosomal dominant entity?
7. Metaphyseal chondrodysplasia, upper limb mesomelia and normal height (mesomelic dysplasia camera type): Second report in a Mexican patient
8. Camptodactyly, joint contractures, facial, and skeletal defects: Further delineation of the Rozin camptodactyly syndrome
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. Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: Further delineation of a new genetic syndrome
12. The Myhre syndrome: report of two cases
13. Poland‐Moebius syndrome in a boy and Poland syndrome in his mother
14. A “new” autosomal dominant genodermatosis characterized by hyperpigmented spots and palmo‐ plantar hyperkeratosis
15. Guadalajara camptodactyly syndrome type II
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