Turner syndrome - Wikipedia
Frontiers | Studying Abnormal Chromosomal Diseases Using Patient-Derived Induced Pluripotent Stem Cells
A Turner Syndrome Patient Carrying a Mosaic Distal X Chromosome Marker – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science hub.
JCDD | Free Full-Text | A Review of Recent Developments in Turner Syndrome Research
Turner syndrome: mechanisms and management | Nature Reviews Endocrinology
Characterization of a rare mosaic X-ring chromosome in a patient with Turner syndrome | Molecular Cytogenetics | Full Text
Clinical and genetic aspects of Turner's syndrome | Medicina Universitaria
TURNER SYNDROME WITH MOSAIC 45, X (77%)/46, XR (X) (23%), (TURNER MOSAIC WITH RING X CHROMOSOME): A CASE REPORT
Molecular cytogenetic characterization of two Turner syndrome patients with mosaic ring X chromosome | SpringerLink
Genetics Behind Turner's | missingxchromosome
Cytogenetic evaluation of patients with clinical spectrum of Turner syndrome Moka R, Sreelakshmi K, Gopinath PM, Satyamoorthy K - J Hum Reprod Sci
An atypical Turner syndrome patient with ring X chromosome mosaicism
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Solved Turner Syndrome Most people who have Turner syndrome | Chegg.com
Spontaneous pregnancy in a 45,X/46,X,r (X) Turner's mosaic patient
Turner syndrome | Oncohema Key
Prenatal diagnosis and molecular cytogenetic identification of small supernumerary marker chromosomes: analysis of three prenatal cases using chromosome microarray analysis | Aging
Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalis - ScienceDirect
Turner's syndrome - The Lancet
JCDD | Free Full-Text | A Review of Recent Developments in Turner Syndrome Research
Clinical Study: XIST Gene and Pattern of X-Inactivation in Children with Ring-X Turner Syndrome | Semantic Scholar
Clinical and genetic aspects of Turner's syndrome - ScienceDirect
LUMEN - Genetics
Features of Turner syndrome among a group of Cameroonian patients - ScienceDirect
