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- The 'D' (13-15) Trisomy Syndrome: an Analysis of 7 Examples G
- Syndrome Review 1: Autosomal Trisomies and Sex Chromosome
- Bleeding Disorders in Congenital Syndromes Susmita N
- SALSA® MLPA® Probemix P245-B1 Microdeletion Syndromes-1A to Be Used with the MLPA General Protocol
- Variants and Health
- A Guide for Parents
- Prenatal Screening for Fetal Aneuploidy AHS – G2055
- 45,X/46,XY/47,XY,+21 Mosaicism in a Hypogonadal Phenotypic Male
- A Mother with Variant Turner Syndrome and Two Daughters with Trisomy X: a Case Report
- HHS Public Access Author Manuscript
- Sex Chromosome Problems Discovered Through Prenatal Testing
- Double Aneuploidy: a Case of Trisomy 21 with XYY
- New Humandouble Trisomy Or Tetrasomy
- NIH Research Plan on Fragile X Syndrome and Associated Disorders
- Diagnostic Testing and Screening
- Multiple Aneuploidies
- Sex Chromosome Abnormalities
- Trisomy 13 — Patau Syndrome
- Triple X Syndrome Also Called Trisomy X
- Syndrome Toll-Free Information and Support Helpline
- Women at Average (Low) Risk for Chromosome Aneuploidy
- NIPT: High Risk for Sex Chromosome Disorder
- Aneuploidy – What Are the Outcomes ?
- Living with Klinefelter Syndrome (47,XXY) Trisomy X (47,XXX) and 47,XYY
- Ophthalmic Manifestations of Tetrasomy 18P
- Triple X Syndrome
- NIPT: Inconclusive Fetal Sex Or Sex Chromosomes
- Explaning Test Results/Karyotypes to Parents
- NIPT Fact Sheet
- First Trimester Screening
- Trisomy 13 – Patau Syndrome
- FMR1 and the Fragile X Syndrome: Human Genome Epidemiology Review Dana C
- Trisomy 13 (Patau Syndrome)
- Table S1. Diseases and Disorders Associated with Structural And/Or Molecular Abnormalities of Chromosome 13
- Fusion Transcripts of Adjacent Genes: New Insights Into the World of Human Complex Transcripts in Cancer
- Theory of Mind Deficits in Children with Fragile X Syndrome
- Fragile X Syndrome
- Functional Genomic Analysis of Novel Microdeletions And
- Cytogenetics Lecture 1: Introduction to Clinical Cytogenetics
- Fragile X Syndrome
- Supplementary Tables and Figures Chromosomal Microarrays for The
- Chromosome Coding EUROCAT July 2011
- Outcome Following Autosomal Monosomy and Multiple Aneuploidy Results by Noninvasive Prenatal Screening
- 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
- The Discovery of Microdeletion Syndromes in the Post-Genomic Era: Review of the Methodology and Characterization of a New 1Q41q42 Microdeletion Syndrome Lisa G
- Trisomy Disorders
- Enhanced Detection of Clinically Relevant Genomic Imbalances Using a Targeted Plus Whole Genome Oligonucleotide Microarray Erin L
- Mosaic Double Trisomy: Down's Syndrome And
- Pallister–Killian Syndrome Versus Trisomy 12P—A Clinical Study of 5 New Cases and a Literature Review
- Rare Partial Trisomy and Tetrasomy of 15Q11-Q13 Associated with Developmental Delay and Autism Spectrum Disorder
- A Review of Trisomy X (47,XXX) Orphanet Pseudoautosomal Region
- Trisomy/Tetrasomy 21 Mosaicism in CVS: Interpretation of Cytogenetic
- The Fragile X Syndrome
- The Effects of Chromosomal Variances. Introducing Sex Chromosomal Anomalies by Cherylann Caspersen
- Consequences of Aneuploidy in Human Fibroblasts with Trisomy 21
- High Risk for Trisomy 18
- Tetrasomy 9P
- A 14 YEAR-OLD GIRL with TURNER SYNDROME of COMPLICATED KARYOTYPE; 45,X/47,XY, + 18,-- 19, +Der(19),T(Y;19) (Q12 ;Pl 3.3)