- Home
- » Tags
- » Mosaic (genetics)
Top View
- Aneuploidy and More in Neural Diversity and Disease
- ACMG Standards and Guidelines for Fragile X Testing
- Case Reports Presumptive 46,XX/46,XY/47,XXY Mosaicism
- Trisomy 14 Mosaicism FTNW
- Allogeneic Stem Cell Transplantation from Donors with Mosaic Turner Syndrome
- U.O.No. 5455/2021/Admn Dated, Calicut University.P.O, 21.05.2021
- A Mother with Variant Turner Syndrome and Two Daughters with Trisomy X: a Case Report
- Clinicians' Guide to Mosaicism
- Chromosomal Mosaicism in Diagnostic Amniotic Fluid Cell Cultures
- Triple X Syndrome Also Called Trisomy X
- Explaning Test Results/Karyotypes to Parents
- Multiclonal Complexity of Pediatric Acute Lymphoblastic Leukemia and the Prognostic Relevance of Subclonal Mutations by Željko Anti , Jiangyan Yu, Simon V
- Research Progress of Chimeric RNA and Health
- Mosaic Uniparental Disomies and Aneuploidies As Large Structural Variants of the Human Genome
- Extra X Chromosome in Mosaic Klinefelter Syndrome Is Associated with a Hematologic Malignancy
- Expanding the Phenotype of Triple X Syndrome
- Mosaicism for Trisomy 21: a Review
- Exploring the Evolution and Adaptive Role of Mosaic Aneuploidy in A
- Chromosomes and Recurrent Miscarriage
- A Case of Trisomy 9 Mosaicism Confirmed by Microarray Test
- Pregnancy and Neonatal Outcomes After Transfer of Mosaic Embryos: a Review
- Epigenetics and Genomics in Klinefelter Syndrome
- A 46, XX / 46, XY Mosaicism Or Chimerism Diagnosed by Karyotyping Mansura Khan1, Mohammad Moniruzzaman2, Fauzia Mohsin3, Ashesh K
- FMR1 Gene Mutations in Patients with Fragile X Syndrome and Obligate Carriers: 30 Years of Experience in Chile
- Mosaic Turner Syndrome Shows Reduced Phenotypic Penetrance in an Adult Population
- Biological and Clinical Significance of Mosaicism in Human
- A Possible Etiology of the Infertile 46XX Male Subject
- On the Variable Effect of Mosaic Normal/Balanced Chromosomal Rearrangements in Man
- Fragile X Syndrome Full Mutation Females at Increased Risk for Mosaic Turner Syndrome: Fragile X Leads to Chromosome Loss
- Paternal Meiotic Origin of Der(21;21)(Q10;Q10) Mosaicism [46,XX/46,XX,Der(21;21)(Q10;Q10), + 21] in a Girl with Mild Down Syndrome
- An Inside Look at Mosaic Findings in Cancer Susceptibility Genes During One Year at a Clinical Diagnostic Laboratory
- Female Chromosome X Mosaicism Is Age-Related and Preferentially Affects the Inactivated X Chromosome
- Clinical Management of Mosaic Results from Preimplantation Genetic Testing for Aneuploidy (PGT-A) of Blastocysts: a Committee Opinion
- The Rate and Spectrum of Mosaic Mutations During Embryogenesis
- Mosaic Variegated Aneuploidy Syndrome
- A Review of Trisomy X (47,XXX) Orphanet Pseudoautosomal Region
- Triple X Syndrome: a Rare Case Entity with Premature Ovarian Failure, Recurrent Abortion and Secondary Infertility
- How Is Mosaicism Diagnosed?
- Fragile X-Associated Tremor/Ataxia Syndrome (Fxtas)
- Antenatal Cytogenetic Testing in Havana, Cuba
- Complex Behavior of Simple Repeats: the Fragile X Syndrome
- The Fragile X Syndrome
- Notch Signaling Expands a Pre-Malignant Pool of T-Cell Acute Lymphoblastic Leukemia Clones Without Affecting Leukemia-Propagating Cell Frequency
- Microrna Publications Flyer All