Genes | Free Full-Text | Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function
The G-banded karyotype. mar = marker chromosome. | Download Scientific Diagram
Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report - International Journal of Reproductive BioMedicine
Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library
Molecular characterization of an analphoid supernumerary marker chromosome derived from 18q22.1→qter in prenatal diagnosis: a case report | Molecular Cytogenetics | Full Text
A supernumerary marker chromosome with a neocentromere derived from 5p14→pter | Journal of Medical Genetics
De novo small supernumerary marker chromosomes detected on 143 000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches - Malvestiti - 2014 - Prenatal Diagnosis - Wiley ...
Male Infertility Associated with a Supernumerary Marker Chromosome
Prenatal diagnosis and molecular cytogenetic identification of small supernumerary marker chromosomes: analysis of three prenatal cases using chromosome microarray analysis | Aging
Prenatal diagnosis and molecular cytogenetic characterization of a familial small supernumerary marker chromosome derived from the acrocentric chromosome 14/22 - ScienceDirect
Tetrasomy 3q26.32-q29 due to a supernumerary marker chromosome in a child with pigmentary mosaicism of Ito
Marker Chromosome - an overview | ScienceDirect Topics
A karyotype of 47,XY,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
Analphoid de novo marker chromosome inv dup(3)(q28qter) with neocentromere in a dysmorphic and developmentally retarded girl | Journal of Medical Genetics
Genetics
A Search for Uniparental Disomy in Carriers of Supernumerary Marker Chromosomes | European Journal of Human Genetics
Biomedicines | Free Full-Text | The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different Chromosomes
G-banded karyotype showing the marker chromosome. | Download Scientific Diagram
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndrome - ScienceDirect
A supernumerary marker chromosome originating from two diVerent regions of chromosome 18
Mosaic Ring-like Small Supernumerary Marker Chromosome and Gene Mutation in a Male With Intermittent Azoospermia: A Rare Case Report - Jianzhong Zhang, Longyu Li, Qiaoqin Li, Zhonglin Cai, Binbin Wang, Jing Wang,
A de novo marker chromosome 15 in a child with isolated developmental delay | SpringerLink
A Familial Small Supernumerary Marker Chromosome 15 Associated with Cryptic Mosaicism with Two Different Additional Marker Chromosomes Derived de novo from Chromosome 9: Detailed Case Study and Implications for Recurrent Pregnancy Loss
Figure 3 | Characterization of a Small Supernumerary Marker Chromosome Derived from Xq28 and 14q11.2 Detected Prenatally
Frontiers | De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue
Figure 1.3 from Small supernumerary marker chromosomes (sSMC) : why do they break, where they break and how to distinguish harmful from harmless sSMC? | Semantic Scholar
![PDF] A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/d632adcfaa0b331c8dc50cd81c619c9aea5210fc/2-Figure1-1.png "PDF] A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome. | Semantic Scholar")
PDF] A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome. | Semantic Scholar
