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1.
Application of a new molecular technique for the genetic evaluation of products of conception.
Prenat Diagn
; 33(1): 32-41, 2013 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-23168908
2.
QF-PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44,727 first-trimester prenatal diagnoses.
Prenat Diagn
; 33(5): 502-8, 2013 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-23606546
3.
Chromosome abnormalities investigated by non-invasive prenatal testing account for approximately 50% of fetal unbalances associated with relevant clinical phenotypes.
Am J Med Genet A
; 152A(6): 1434-42, 2010 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-20503318
4.
Response to "QF-PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44 727 first-trimester prenatal diagnoses".
Prenat Diagn
; 33(11): 1117, 2013 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-24590588
5.
Quantitative fluorescence-polymerase chain reaction assay for the detection of the duplication of the Charcot Marie Tooth disease type 1A critical region.
Genet Test Mol Biomarkers
; 14(2): 225-31, 2010 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-20187762
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