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Prenatal diagnosis and molecular cytogenetic characterization of a familial  small supernumerary marker chromosome derived from the acrocentric  chromosome 14/22 - ScienceDirect
Prenatal diagnosis and molecular cytogenetic characterization of a familial small supernumerary marker chromosome derived from the acrocentric chromosome 14/22 - ScienceDirect

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
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

A new small supernumerary marker chromosome, generating mosaic pure trisomy  16q11.1–q12.1 in a healthy man | Molecular Cytogenetics | Full Text
A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1–q12.1 in a healthy man | 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
Molecular characterization of an analphoid supernumerary marker chromosome derived from 18q22.1→qter in prenatal diagnosis: a case report | Molecular Cytogenetics | Full Text

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
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

Molecular cytogenetic characterization of mosaicism for a small  supernumerary marker chromosome derived from chromosome 8 or  r(8)(::p12→q13.1::) associated with phenotypic abnormalities - ScienceDirect
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities - ScienceDirect

A supernumerary marker chromosome with a neocentromere derived from  5p14→pter | Journal of Medical Genetics
A supernumerary marker chromosome with a neocentromere derived from 5p14→pter | Journal of Medical Genetics

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

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

Small supernumerary marker chromosome - Wikipedia
Small supernumerary marker chromosome - Wikipedia

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

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

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

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Genetics

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

The G-banded karyotype. mar = marker chromosome. | Download Scientific  Diagram
The G-banded karyotype. mar = 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
Biomedicines | Free Full-Text | The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different Chromosomes

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

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

Figure 2 | Anatomical Asplenia in Cat Eye Syndrome: An Expansion of the  Disease Spectrum
Figure 2 | Anatomical Asplenia in Cat Eye Syndrome: An Expansion of the Disease Spectrum

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

A de novo marker chromosome 15 in a child with isolated developmental delay  | SpringerLink
A de novo marker chromosome 15 in a child with isolated developmental delay | SpringerLink