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Tetrasomy 9p
First Case Report of Maternal Mosaic Tetrasomy 9P Incidentally Detected on Non-Invasive Prenatal Testing
Mosaic Tetrasomy 9P at Amniocentesis: Prenatal Diagnosis, Molecular Cytogenetic Characterization, and Literature Review
CYTOGENETICS: Rotation Director: Robert Zori, M
Tetrasomy 9P Syndrome in a Filipino Infant
Orphanet Report Series Rare Diseases Collection
Inside This Issue
Early ACCESS Diagnosed Conditions List
Congenital Knee Dislocation in a 49,XXXXY Boy J Med Genet: First Published As 10.1136/Jmg.32.4.309 on 1 April 1995
Mosaic Tetrasomy of 9P24.3Q21.11 Postnatally Identified in an Infant
Trisomy 9 Mosaicism FTNW
Duplications of 9P
Mosaic Tetrasomy 9P Case with the Phenotype Mimicking Klinefelter Syndrome and Hyporesponse of Gonadotropin-Stimulated Testosterone Production
Percept Is Different
Backup of جلد پی دی اف.Cdr
Genetic Studies of Autism Spectrum Disorder in Asians
Clinical and Molecular Delineation of Tetrasomy 9P Syndrome
NIPT – Not Invariably Perfect Test
Nuove Politiche Per L'innovazione Nel Settore Delle Scienze Della Vita
Top View
Review Article
Case Reports
Co-Existing 9P Duplication & Deletion
(12) Patent Application Publication (10) Pub. No.: US 2007/0135335 A1 Collier Et Al
The Principles of Clinical Cytogenetics
Cytogenomics Conference 2019 Salzburg, Austria
Sonographic Findings in a Case of Tetrasomy 9P Associated with Increased Nuchal Translucency and Dandy-Walker Malformation
Attention Deficit Disorder in the Neuropediatric Outpatient Clinic
Fabio Pammolli, Massimo Riccaboni, Laura Magazzini, Mark Supekar
Posterpresentations
Therapeutic and Diagnostic Agents
9 Chromosome Chapter
Tetrasomy 9P Confirmed by GALT
Type 1 Established Condition List
Non-Mosaic Tetrasomy 9P in an Infant with Multiple Congenital Anomalies
Danişman Prof. Dr. Seher Başaran Genetik Anabilim Dali Genetik Programi Istanbul-2011 Güven Toksoy Fetal Kromozom An
Small Supernumerary Marker Chromosomes and Their Correlation with Specific Syndromes
Cals (O) (5) (O) - (E)------O O Ocs) Iningas
Mosaic Chromosomal Aneuploidy Detection by Sequencing (MAD-Seq)
Prevalence and Incidence of Rare Diseases: Bibliographic Data
Prevalence and Incidence of Rare Diseases
A Genome Wide Scan for Familial High Myopia Suggests a Novel Locus On
Teeth Common Concerns FTNW
Established Conditions List
Esit Diagnosis List
Orphanet Report Series Rare Diseases Collection
Tetrasomy 9P