Molecular cytogenetic characterization of two Turner syndrome patients with mosaic ring X chromosome | SpringerLink
Cytogenetic evaluation of patients with clinical spectrum of Turner syndrome Moka R, Sreelakshmi K, Gopinath PM, Satyamoorthy K - J Hum Reprod Sci
Clinical Study: XIST Gene and Pattern of X-Inactivation in Children with Ring-X Turner Syndrome | Semantic Scholar
A) showing short fourth metacarpal in left hand skiagram (yellow... | Download Scientific Diagram
Solved Turner Syndrome Most people who have Turner syndrome | Chegg.com
Lack of expression of XIST from a small ring X chromosome containing the XIST locus in a girl with short stature, facial dysmorphism and developmental delay | European Journal of Human Genetics
Clinical Study: XIST Gene and Pattern of X-Inactivation in Children with Ring-X Turner Syndrome | Semantic Scholar
Features of Turner syndrome among a group of Cameroonian patients - ScienceDirect
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Karyotype of patient shows classic Turner syndrome 45,X | Download Scientific Diagram
TURNER SYNDROME WITH MOSAIC 45, X (77%)/46, XR (X) (23%), (TURNER MOSAIC WITH RING X CHROMOSOME): A CASE REPORT
A Turner syndrome woman with a ring X chromosome [45,X/46,X,r(X)(p22.3q27)] whose child also had a ring X chromosome
Prenatal diagnosis and molecular cytogenetic identification of small supernumerary marker chromosomes: analysis of three prenatal cases using chromosome microarray analysis | Aging
Turner syndrome: MedlinePlus Genetics
Turner syndrome: mechanisms and management | Nature Reviews Endocrinology
Turner's syndrome - The Lancet
Spontaneous pregnancy in a 45,X/46,X,r (X) Turner's mosaic patient
View of Isochromosome Mosaic Turner Syndrome | Journal of the ASEAN Federation of Endocrine Societies
Frontiers | Studying Abnormal Chromosomal Diseases Using Patient-Derived Induced Pluripotent Stem Cells
JCDD | Free Full-Text | A Review of Recent Developments in Turner Syndrome Research
Genetics Behind Turner's | missingxchromosome
Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalis - ScienceDirect
A short ring finger points to a diagnosis of Turner syndrome again - The Lancet
LUMEN - Genetics
Clinical and genetic aspects of Turner's syndrome - ScienceDirect
