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Trisomy X
Sema4 Noninvasive Prenatal Select
Structural and Numerical Changes of Chromosome X in Patients with Esophageal Atresia
Example Document Medical Genetics Center
Inside This Issue
Prenatal Diagnosis by FISH of a 22Ql 1 Deletion in Two Families J Med Genet: First Published As 10.1136/Jmg.35.2.165 on 1 February 1998
Double Aneuploidy in Down Syndrome
Female Polysomy-X and Systemic Lupus Erythematosus
Curriculum Vitae
Original Article
Early ACCESS Diagnosed Conditions List
Uniparental Disomy of the Entire X Chromosome in Turner Syndrome Patient-Specific Induced Pluripotent Stem Cells
Case Report Genetic Counseling for Trisomy X Syndrome Diagnosed By
Triple X Syndrome with a Rare Finding: Cleft Palate
Acta Nr. 4 2012.Qxd
Trisomy X) • AXYS Family Conference • 48,XXYY and 48,XXXY
The Physical and Genetic Components of Intersex
Syndrome Review 1: Autosomal Trisomies and Sex Chromosome
General Information About Positive NIPT Results
Top View
Medical Sciences
Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population
A Guide for Parents
X Chromosome Fact Sheet
The Challenges of Clinical Trials in Fragile X Syndrome
Mosaic Male Fetus with Retained XIST Gene
47,XYY Syndrome Complications Other Names: • Increased Risk of Learning Disabilities • Delayed Development of Speech and Language • Jacob’S Syndrome Skills
Turner Syndrome and Its Variants Turner Sendromu Ve Varyantları
Cytogenetic Findings in Patients with Intellectual Disability/Mental Retardation and Dysmorphic Features in Eastern Croatia 1
Near Tetraploidy in a Patient with Systemic Lupus Erythematosus Nine 249 Μmol/L)
Triple X Syndrome Also Called Trisomy X
Syndrome Toll-Free Information and Support Helpline
NIPT: High Risk for Sex Chromosome Disorder
Triple X Syndrome Woman Presenting As Premature Ovarian Failure
Living with Klinefelter Syndrome (47,XXY) Trisomy X (47,XXX) and 47,XYY
Triple X Syndrome
NIPT: Inconclusive Fetal Sex Or Sex Chromosomes
Expanding the Phenotype of Triple X Syndrome
Double Aneuploidy 48,ХХХ,+21 of a Bulgarian Newborn with Down
Noninvasive Prenatal Genetic Testing for Fetal Aneuploidy Detects Maternal Trisomy X
Type 1 Established Condition List
Childhood-Onset Systemic Lupus Erythematosus with Trisomy X and the Increased Risk for Bone Complications: a Case Report
Booklet: for Extra Special Girls – a Guide to Trisomy X (47,XXX)
COMMON Aneuploidy and Microdeletion Syndromes
From the Handbook of Pediatric Neuropsychology
Triple-X-Syndrome Or Trisomy X
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
My Guide to Trisomy X Dear Parents
Cognitive and Neurological Aspects of Sex Chromosome Aneuploidies
Triple-X Syndrome Accompanied by a Single Maxillary Central
Trisomy Xp and Partial Tetrasomy Xq Resulting from Gain of a Rearranged
The Effects of Chromosomal Variances. Introducing Sex Chromosomal Anomalies by Cherylann Caspersen