Alliende MA - Search Results

1

FMR1 gene mutations in patients with fragile X syndrome and obligate carriers: 30 years of experience in Chile.

Santa María L, Aliaga S, Faundes V, Morales P, Pugin Á, Curotto B, Soto P, Peña MI, Salas I, Alliende MA. Santa María L, et al. Among authors: alliende ma. Genet Res (Camb). 2016 Jun 28;98:e11. doi: 10.1017/S0016672316000082. Genet Res (Camb). 2016. PMID: 27350105 Free PMC article.

2

FXTAS in an unmethylated mosaic male with fragile X syndrome from Chile.

Santa María L, Pugin A, Alliende MA, Aliaga S, Curotto B, Aravena T, Tang HT, Mendoza-Morales G, Hagerman R, Tassone F. Santa María L, et al. Among authors: alliende ma. Clin Genet. 2014 Oct;86(4):378-82. doi: 10.1111/cge.12278. Epub 2013 Oct 13. Clin Genet. 2014. PMID: 24028275 Free PMC article.

3

Clinical, molecular, and pharmacological aspects of FMR1 related disorders.

Pugin A, Faundes V, Santa María L, Curotto B, Aliaga S, Salas I, Soto P, Bravo P, Peña MI, Alliende MA. Pugin A, et al. Among authors: alliende ma. Neurologia. 2017 May;32(4):241-252. doi: 10.1016/j.nrl.2014.10.009. Epub 2014 Dec 17. Neurologia. 2017. PMID: 25529181 Free article. Review. English, Spanish.

4

Molecular classes in 209 patients with Prader-Willi or Angelman syndromes: lessons for genetic counseling.

Faundes V, María LS, Aliaga S, Curotto B, Pugin A, Alliende MA. Faundes V, et al. Among authors: alliende ma. Am J Med Genet A. 2015 Jan;167A(1):261-3. doi: 10.1002/ajmg.a.36801. Epub 2014 Oct 6. Am J Med Genet A. 2015. PMID: 25287901 No abstract available.

5

Comparison of two subtelomeric assays for the screening of chromosomal rearrangements: analysis of 383 patients, literature review and further recommendations.

Santa María L, Faundes V, Curotto B, Morales P, Morales K, Aliaga S, Pugin Á, Alliende MA. Santa María L, et al. Among authors: alliende ma. J Appl Genet. 2016 Feb;57(1):63-9. doi: 10.1007/s13353-015-0295-4. Epub 2015 Jun 12. J Appl Genet. 2016. PMID: 26069167 Review.

6

[Microarrays in 236 patients with neurodevelopmental disorders and congenital abnormalities].

Faundes V, Santa María L, Morales P, Curotto B, Alliende MA. Faundes V, et al. Among authors: alliende ma. Rev Med Chil. 2017 Jul;145(7):854-861. doi: 10.4067/s0034-98872017000700854. Rev Med Chil. 2017. PMID: 29182193 Free article. Spanish.

7

[Direct molecular analysis of FMR-1 gene mutation in patients with fragile Xq syndrome and their families].

Alliende MA, Urzúa B, Valiente A, Cortés F, Curotto B, Rojas C. Alliende MA, et al. Rev Med Chil. 1998 Dec;126(12):1435-46. Rev Med Chil. 1998. PMID: 10349157 Spanish.

8

[Cytogenetic findings in patients with Down's syndrome].

Cortés F, Alliende M, Curotto B. Cortés F, et al. Rev Chil Pediatr. 1990 Nov-Dec;61(6):313-6. Rev Chil Pediatr. 1990. PMID: 2152215 Spanish.

9

[Genetic screening to determine an etiologic diagnosis in children with mental retardation].

Alliende MA, Cámpora L, Curotto B, Toro J, Valiente A, Castillo M, Cortés F, Trigo C, Alvarado C, Silva M, Caru M. Alliende MA, et al. Rev Med Chil. 2008 Dec;136(12):1542-51. Epub 2009 Mar 23. Rev Med Chil. 2008. PMID: 19350171 Free article. Spanish.

10

[Cytogenetic and molecular profile of genetic diseases in Puerto Montt main hospital].

Alliende MA, Curotto B, Guerra P, Santa María L, Hermosilla R, Orphanópoulos D, Villanueva J, Wettig E, Barraza X. Alliende MA, et al. Rev Med Chil. 2011 Mar;139(3):298-305. Epub 2011 Aug 25. Rev Med Chil. 2011. PMID: 21879160 Free article. Spanish.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

20 results

Search Page

Filters