Keywords: Products of conception (POC); Culture failure; Normal karyotype; Array comparative genomic hybridization (aCGH); Chromosomal and genomic abnormalities; Apoptosis
مقالات ISI (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Distribution patterns of segmental aneuploidies in human blastocysts identified by next-generation sequencing
Keywords: Array comparative genomic hybridization (aCGH); blastocyst; mosaicism; next-generation sequencing; segmental aneuploidy;
Genomic and genetic variation in E2F transcription factor-1 in men with nonobstructive azoospermia
Keywords: Azoospermia; E2F1; infertility; NOA; cryptorchidism; array comparative genomic hybridization (aCGH); copy number variations (CNV);
Targeted array comparative genomic hybridization - A new diagnostic tool for the detection of large copy number variations in nemaline myopathy-causing genes
Keywords: Nebulin; NEB; Array comparative genomic hybridization (aCGH); NM-CGH; Copy number variation; Deletion; Nemaline myopathy;
A feasible strategy of preimplantation genetic diagnosis for carriers with chromosomal translocation: Using blastocyst biopsy and array comparative genomic hybridization
Keywords: array comparative genomic hybridization (aCGH); blastocyst biopsy; chromosomal translocation; infertility; preimplantation genetic diagnosis (PGD)
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4
Keywords: Array comparative genomic hybridization (aCGH); Chromosome 4; Mosaicism; Prenatal diagnosis; Ring chromosome; Small supernumerary marker chromosome (sSMC); Spectral karyotyping (SKY)
Contiguous gene deletion syndrome in a female with ornithine transcarbamylase deficiency
Keywords: Ornithine transcarbamylase (OTC); Contiguous gene deletion syndrome; Multiplex ligation-dependent probe amplification (MLPA); Array comparative genomic hybridization (aCGH); Skewed X-inactivation
Proximal interstitial 1p36 deletion syndrome: The most proximal 3.5-Mb microdeletion identified on a dysmorphic and mentally retarded patient with inv(3)(p14.1q26.2)
Keywords: Proximal interstitial deletion of 1p36; Array comparative genomic hybridization (aCGH); Fluorescence in situ hybridization (FISH); Inversion; Cryptic deletion; Low copy repeats
Manifestation, mechanisms and mysteries of gene amplifications
Keywords: Amplification; Cancer; Array comparative genomic hybridization (aCGH); Databases; Systems biology