Partial trisomy 2q33.3-q37.3 in a patient with an inverted duplicated neocentric marker chromosome | Molecular Cytogenetics | Full Text
A de novo marker chromosome 15 in a child with isolated developmental delay | SpringerLink
A unique case of female pseudohermaphroditism with 21-hydroxylase deficiency and small supernumerary marker chromosome 7
CHARACTERISATION OF MARKER CHROMOSOMES | PharmaTutor
G-banded karyotype showing the marker chromosome. | Download Scientific Diagram
A karyotype of 47,XX,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
Characterization of a Small Supernumerary Marker Chromosome Derived from Xq28 and 14q11.2 Detected Prenatally
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11 - ScienceDirect
SciELO - Brasil - Tetrasomy 3q26.32-q29 due to a supernumerary marker chromosome in a child with pigmentary mosaicism of Ito Tetrasomy 3q26.32-q29 due to a supernumerary marker chromosome in a child with
The G-banded karyotype. mar = marker chromosome. | Download Scientific Diagram
Male Infertility Associated with a Supernumerary Marker Chromosome
CHARACTERISATION OF MARKER CHROMOSOMES | PharmaTutor
A karyotype of 47,XX,þmar. The arrow indicates a marker chromosome (mar). | Download Scientific Diagram
Genes | Free Full-Text | Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function | HTML
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A novel translocation der(4)t(1;4)(q21;q35) and a marker chromosome in a case of myelodysplastic syndrome - Cancer Genetics and Cytogenetics
A supernumerary marker chromosome with a neocentromere derived from 5p14→pter | Journal of Medical Genetics
CHARACTERISATION OF MARKER CHROMOSOMES | PharmaTutor
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15. | Semantic Scholar
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Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
