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Tetrasomy 18p
Association of Congenital Diaphragmatic Hernia and Hiatal Hernia with Tetrasomy 18P
Prenatal Diagnosis of Mosaic Tetrasomy 18P in a Case Without Sonographic Abnormalities
Tetrasomy 18P: Case Report and Review of Literature
Epilepsy and Chromosome 18 Abnormalities: a Review
Tetrasomy 18P
Chromosome Microarray Testing (Non-Oncology Conditions) – Oxford Clinical Policy
Pallister-Killian Syndrome
CMJ a Female Infant Case with Tetrasomy 18P Bir Dişi
18 Chromosome Chapter
Clinical and Molecular Delineation of Tetrasomy 9P Syndrome
A Rare Chromosomal Disorder – Isochromosome 18P Syndrome
A Small Supernumerary Marker Chromosome Resulting in Mosaic Partial Tetrasomy 4Q26-Q31.21 in a Fetus with Multiple Congenital Malformations
Code Disease Name
List Rare Diseases.Txt
(12) Patent Application Publication (10) Pub. No.: US 2007/0135335 A1 Collier Et Al
Clinical and Molecular Findings in Nine New
Therapeutic and Diagnostic Agents
Trisomy 18P Treatment and Surveillance ICD-10 =Q93.2
Top View
Type 1 Established Condition List
Tetrasomy 18P Treatment and Surveillance ICD-10 =Q93.2
Proximal 18Q
A Case of Partial Trisomy 2P23-Pter Syndrome with Trisomy 18P Due to a De Novo Supernumerary Marker Chromosome
Isochromosome 18P
Treatment of Dysphagia in Children with Rare Disorders: Problem Solving, Collaboration and Treatment Planning in the Unknown
Tetrasomy 18P
Clinical and Cytogenetic Characterization of a Patient with Tetrasomy 18P Caracterización Clínica Y Citogenética De Un Paciente Con Tetrasomía 18P
Two Cases of Isochromosome 18Q Syndrome Pal S, Siti M I, Ankathil R, Zilfalil B A
Prenatal Diagnosis of Mosaic Tetrasomy 18P
Trisomy 18 Phenotype in a Patient with an Isopseudodicentric 18 Chromosorne*
Tetrasomy 18P : Tentative Delineation of a Syndrome
Orphanet Report Series Rare Diseases Collection