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Spoločný výber študent Hviezda marker chromosome vyčistiť ťahať odporný

A Search for Uniparental Disomy in Carriers of Supernumerary Marker  Chromosomes | European Journal of Human Genetics
A Search for Uniparental Disomy in Carriers of Supernumerary Marker Chromosomes | European Journal of Human Genetics

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

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

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Hypogonadotropic hypogonadism associated with another small supernumerary marker  chromosome (sSMC) derived from chromosome 22, a case report - Abdullah -  Translational Andrology and Urology
Hypogonadotropic hypogonadism associated with another small supernumerary marker chromosome (sSMC) derived from chromosome 22, a case report - Abdullah - Translational Andrology and Urology

Marker Chromosomes | SpringerLink
Marker Chromosomes | 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
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

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

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

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

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

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

Analphoid de novo marker chromosome inv dup(3)(q28qter) with neocentromere  in a dysmorphic and developmentally retarded girl | Journal of Medical  Genetics
Analphoid de novo marker chromosome inv dup(3)(q28qter) with neocentromere in a dysmorphic and developmentally retarded girl | Journal of Medical Genetics

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

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

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

Case 613 -- Cytogenetics - Pathology Case
Case 613 -- Cytogenetics - Pathology Case

menetrend Várj egy percet Levelek gyűjtése marker cromosom És a csapat  Confuse Plüss Doll
menetrend Várj egy percet Levelek gyűjtése marker cromosom És a csapat Confuse Plüss Doll

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

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

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

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

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

Characterization of giant marker and ring chromosomes in a pleomorphic  leiomyosarcoma of soft tissue by spectral karyotyping
Characterization of giant marker and ring chromosomes in a pleomorphic leiomyosarcoma of soft tissue by spectral karyotyping