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The G-banded karyotype. mar = marker chromosome. | Download Scientific  Diagram
The G-banded karyotype. mar = marker chromosome. | Download Scientific Diagram

A karyotype of 47,XX,þmar. mar ¼ marker chromosome. | Download Scientific  Diagram
A karyotype of 47,XX,þmar. mar ¼ marker chromosome. | Download Scientific Diagram

Molecular characterization of an analphoid supernumerary marker chromosome  derived from 18q22.1→qter in prenatal diagnosis: a case report | Molecular  Cytogenetics | Full Text
Molecular characterization of an analphoid supernumerary marker chromosome derived from 18q22.1→qter in prenatal diagnosis: a case report | Molecular Cytogenetics | Full Text

Small supernumerary marker chromosomes: A legacy of trisomy rescue? -  Kurtas - 2019 - Human Mutation - Wiley Online Library
Small supernumerary marker chromosomes: A legacy of trisomy rescue? - Kurtas - 2019 - Human Mutation - Wiley Online Library

A supernumerary marker chromosome originating from two different regions of  chromosome 18 | Journal of Medical Genetics
A supernumerary marker chromosome originating from two different regions of chromosome 18 | Journal of Medical Genetics

A karyotype of 47,XY,þmar. mar ¼ marker chromosome. | Download Scientific  Diagram
A karyotype of 47,XY,þmar. mar ¼ marker chromosome. | Download Scientific Diagram

Figure 3 | Characterization of a Small Supernumerary Marker Chromosome  Derived from Xq28 and 14q11.2 Detected Prenatally
Figure 3 | Characterization of a Small Supernumerary Marker Chromosome Derived from Xq28 and 14q11.2 Detected Prenatally

A karyotype of 47,XY,þmar. mar ¼ marker chromosome. | Download Scientific  Diagram
A karyotype of 47,XY,þmar. mar ¼ marker chromosome. | 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
Genes | Free Full-Text | Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome in Patients with Impaired Reproductive Function

Male Infertility Associated with a Supernumerary Marker Chromosome
Male Infertility Associated with a Supernumerary Marker Chromosome

Neocentromere - Wikipedia
Neocentromere - Wikipedia

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
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

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
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

Biomedicines | Free Full-Text | The First Neocentric, Discontinuous, and  Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic  Blocks Derived from 5 Different Chromosomes
Biomedicines | Free Full-Text | The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different Chromosomes

PDF] Small supernumerary marker chromosomes (sSMC) in humans | Semantic  Scholar
PDF] Small supernumerary marker chromosomes (sSMC) in humans | Semantic Scholar

Frontiers | Case Report: Genetic Analysis of a Small Supernumerary Marker  Chromosome in a Unique Case of Mosaic Turner Syndrome
Frontiers | Case Report: Genetic Analysis of a Small Supernumerary Marker Chromosome in a Unique Case of Mosaic Turner Syndrome

Molecular cytogenetic characterization of small supernumerary marker 15 in  infertile male: A case report
Molecular cytogenetic characterization of small supernumerary marker 15 in infertile male: A case report

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
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

Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal  samples: chromosomal distribution, clinical findings, and UPD studies |  European Journal of Human Genetics
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics

Marker Chromosomes | SpringerLink
Marker Chromosomes | SpringerLink

Cytogenomic Characterization of Giant Ring or Rod Marker Chromosome in Four  Cases of Well-Differentiated and Dedifferentiated Liposarcoma
Cytogenomic Characterization of Giant Ring or Rod Marker Chromosome in Four Cases of Well-Differentiated and Dedifferentiated Liposarcoma

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Marker Chromosome - an overview | ScienceDirect Topics
Marker Chromosome - an overview | ScienceDirect Topics

First case of two supernumerary markers derived from chromosome 5 and  chromosome 8 | Molecular Cytogenetics | Full Text
First case of two supernumerary markers derived from chromosome 5 and chromosome 8 | Molecular Cytogenetics | Full Text

Prenatal diagnosis of de novo small supernumerary marker chromosome 4q  (4q11-q12): A case report - International Journal of Reproductive  BioMedicine
Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report - International Journal of Reproductive BioMedicine

The Use of Molecular Cytogenetic Techniques for the Identification of  Chromosomal Abnormalities | IntechOpen
The Use of Molecular Cytogenetic Techniques for the Identification of Chromosomal Abnormalities | IntechOpen