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Tetrasomy X
The National Economic Burden of Rare Disease Study February 2021
Klinefelter Syndrome) at 9 Years of Age
Orphanet Report Series Rare Diseases Collection
Inside This Issue
Female Polysomy-X and Systemic Lupus Erythematosus
Genetic Evaluation of Inpatient Neonatal and Infantile Congenital Heart Defects: New Findings and Review of the Literature
The Frequency of Aneuploidy in Cultured Lymphocytes Is Correlated with Age and Gender but Not with Reproductive History
Acta Nr. 4 2012.Qxd
Tetrasomy X in a Child with Multiple Abnormalities: Case Report and Literature Review from China
Erciyes Medical Genetics Days 2019
Effects of Human Sex Chromosome Dosage on Spatial Chromosome Organization
The Type and Prevalence of Chromosomal Abnormalities in Couples
ORPHA Number Disease Or Group of Diseases 300305 11P15.4
Mosaic Pentasomy X/Tetrasomy X Syndrome and Premature Ovarian Failure
Tetrasomy X FTNW
Triple X Syndrome Also Called Trisomy X
Modeling Down Syndrome Neurodevelopment with Dosage Compensation
Living with Klinefelter Syndrome (47,XXY) Trisomy X (47,XXX) and 47,XYY
Top View
48,Xxxx, a Rare Aneuploidy
The Extraordinary Kids Clinic: an Interdisciplinary Model of Care for Children and Adolescents with Sex Chromosome Aneuploidy
Pentasomy X FTNP
Array-CGH Revealed Gain of Yp11. 2 in 49, XXXXY and Gain of Xp22. 33 In
Fusion Transcripts of Adjacent Genes: New Insights Into the World of Human Complex Transcripts in Cancer
Appendix B: List of Rare Diseases
Tetrasomy X, a Rare Cause of Epilepsy and Behavior Disorder
Understanding Chromosome Disorders and Their Implications for Special Educators
Application of Chromosomal Microarray Analysis in Products Of
From the Handbook of Pediatric Neuropsychology
Prevalence and Incidence of Rare Diseases: Bibliographic Data
Prevalence and Incidence of Rare Diseases
A Review of Trisomy X (47,XXX) Orphanet Pseudoautosomal Region
Teeth Common Concerns FTNW
Parental Origin and Cell Stage Errors in X-Chromosome Polysomy 49,Xxxxy
Orphanet Report Series Rare Diseases Collection
Tetrasomy X in a Child with Upper Limb Deformity