Home

být zticha Netolerovatelné zaneprázdněný marker chromozome Paměť Díkůvzdání odolat

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

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

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

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

A Small Supernumerary Marker Derived from the Pericentromeric Region of  Chromosome 5: Case Report and Delineation of Partial Trisomy 5p Phenotype |  Semantic Scholar
A Small Supernumerary Marker Derived from the Pericentromeric Region of Chromosome 5: Case Report and Delineation of Partial Trisomy 5p Phenotype | Semantic Scholar

OBM Genetics | Identification of a Small Supernumerary Marker Chromosome  Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular  Characterization
OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization

At chromosome level - Genetics - UZ Brussel
At chromosome level - Genetics - UZ Brussel

Frontiers | De Novo Small Supernumerary Marker Chromosomes Arising From  Partial Trisomy Rescue
Frontiers | De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue

Prenatal diagnosis and molecular cytogenetic characterization of a small  supernumerary marker chromosome (sSMC) inherited from her mosaic sSMC(15)  mother and a literature review - ScienceDirect
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome (sSMC) inherited from her mosaic sSMC(15) mother and a literature review - ScienceDirect

Small supernumerary marker chromosomes derived from chromosome 14 and/or 22  | Molecular Cytogenetics | Full Text
Small supernumerary marker chromosomes derived from chromosome 14 and/or 22 | Molecular Cytogenetics | Full Text

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

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

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

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

Genetics
Genetics

Marker Chromosomes | SpringerLink
Marker Chromosomes | SpringerLink

Home
Home

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

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

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

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

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