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Noninvasive prenatal diagnosis using ccffDNA in maternal blood: state of the art.
Expert Rev Mol Diagn. 2010 Mar;10(2):197-205. doi: 10.1586/erm.09.86.
Expert Rev Mol Diagn. 2010.
PMID: 20214538
Review.
Broadening our understanding by the use of molecular cytogenetic techniques: full monosomy 21.
Martinez-Garcia M, Ainse E, García-Hoyos M, Bustamante A, Cardero R, Ramos-Corrales C, Trujillo-Tiebas MJ, de Alba MR, Lorda I.
Martinez-Garcia M, et al. Among authors: ainse e.
J Assist Reprod Genet. 2011 Jul;28(7):621-6. doi: 10.1007/s10815-011-9569-x. Epub 2011 May 4.
J Assist Reprod Genet. 2011.
PMID: 21573680
Free PMC article.
No abstract available.
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Novel human pathological mutations. Gene symbol: GUCY2D. Disease: Leber congenital amaurosis.
Auz-Alexandre CL, Vallespin E, Aguirre-Lamban J, Cantalapiedra D, Avila-Fernandez A, Villaverde-Montero C, Ainse E, Trujillo-Tiebas MJ, Ayuso C.
Auz-Alexandre CL, et al. Among authors: ainse e.
Hum Genet. 2009 Apr;125(3):349.
Hum Genet. 2009.
PMID: 19320033
No abstract available.
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