OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization
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,
Biomedicines | Free Full-Text | Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing
The algorithm for the determination of chromosomal origin of marker... | Download Scientific Diagram
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
Genes | Free Full-Text | Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function
Formation of Small Supernumerary Marker Chromosomes | SpringerLink
A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1–q12.1 in a healthy man | Molecular Cytogenetics | Full Text
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
Solved Whole chromosome paints are useful in the following | Chegg.com
Chromothripsis Detectable in Small Supernumerary Marker Chromosomes (sSMC) Using Fluorescence In Situ Hybridization (FISH) | SpringerLink
Molecular delineation of small supernumerary marker chromosomes using a single nucleotide polymorphism array | Molecular Cytogenetics | Full Text
Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library
Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient | Scientific Reports
Identification of small marker chromosomes using microarray comparative genomic hybridization and multicolor fluorescent in situ hybridization | Molecular Cytogenetics | Full Text
Small supernumerary marker chromosome - Wikipedia
Frontiers | Case Report: Genetic Analysis of a Small Supernumerary Marker Chromosome in a Unique Case of Mosaic Turner Syndrome
A supernumerary marker chromosome with a neocentromere derived from 5p14→pter | Journal of Medical Genetics
Frontiers | De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue
A karyotype of 47,XX,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
Biomedicines | Free Full-Text | The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different Chromosomes
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
The G-banded karyotype of 47,XY,þmar. mar ¼ marker chromosome. | Download Scientific Diagram
G-banded karyotype showing the marker chromosome. | Download Scientific Diagram
FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22) | European Journal of Human Genetics
Parental origin of multiple small supernumerary marker chromosomes: evidence from a rare prenatal and postnatal case – тема научной статьи по биологическим наукам читайте бесплатно текст научно-исследовательской работы в электронной библиотеке КиберЛенинка
