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- Prenatal Diagnosis of True Fetal Mosaicism with Small
- And Uniparental Disomy (UPD): Coincidence Or Consequence? D Kotzot
- A Systematic Analysis of Small Supernumerary Marker Chromosomes Using Array CGH Exposes Unexpected Complexity
- Easychip 8X15k
- FISH of Supernumerary Marker Chromosomes (Smcs) Identifies Six Diagnostically Relevant Intervals on Chromosome 22Q and a Novel Type of Bisatellited SMC(22)
- 10Th European Cytogenetics Conference 2015 4–7 July 2015, Strasbourg – France
- PDF Hosted at the Radboud Repository of the Radboud University Nijmegen
- Small Supernumerary Marker Chromosomes Derived from Chromosomes 6 and 20 in a Woman with Recurrent Spontaneous Abortions
- A Placental Trisomy 2 Detected by NIPT Evolved in a Fetal Small Supernumerary Marker Chromosome (Ssmc)
- Supernumerary Marker Chromosome in a Child with Microcephaly and Mental Retardation
- Small Supernumerary Markerchromosomes (Ssmc)
- Prenatal Diagnosis and Genetic Counseling in a Fetus Associated
- Maternal UPD 20 in a Hyperactive Child with Severe Growth Retardation
- The Internet Page on Small Supernumerary Marker Chromosomes (Ssmc)
- Partial Tetrasomy 12Pter-12P12.3 in a Girl with Pallister-Killian Syndrome: Extraordinary Finding of an Analphoid, Inverted Duplicated Marker
- Chromosome Rearrangements Discovered Through Prenatal
- Array Comparative Genomic Hybridisation in Clinical Diagnostics: Principles and Applications Array-CGH in Der Klinischen Diagnostik: Prinzipien Und Anwendungen
- Cytogenetic Variation of B-Lymphoblastic Leukemia with Intrachromosomal Amplification of Chromosome 21 (Iamp21) a Multi-Institutional Series Review
- Skin Pigmentary Anomalies and Mosaicism for an Acentric Marker
- PARP3 Is a Promoter of Chromosomal Rearrangements and Limits G4 DNA
- Forty-Two Supernumerary Marker Chromosomes (Smcs) in 43 273 Prenatal Samples: Chromosomal Distribution, Clinical Findings, and UPD Studies
- Fetal Loss: a Genetic Insight of the De Novo Accessory Bi-Satellited
- Clinical and Molecular Findings in Nine New
- Duplications of FOXG1 in 14Q12 Are Associated with Developmental Epilepsy, Mental Retardation, and Severe Speech Impairment
- Molecular Characterization of Microduplication 22Q11.2 in a Girl with Hypernasal Speech
- Congenital Malformations in a Holstein-Fresian Calf with a Unique Mosaic Karyotype: a Case Report
- A Supernumerary Marker Chromosome 15 Tetrasomic for the Prader-Willi
- Male Infertility Associated with a Supernumerary Marker Chromosome
- Chromosomal Variants in Klinefelter Syndrome
- Novel Phenotype of 5P13.3-Q11.2 Duplication Resulting from Supernumerary Marker Chromosome 5: Implications for Management and Genetic Counseling Margaret E
- Two Separate Cases: Complex Chromosomal Abnormality Involving Three Chromosomes and Small Supernumerary Marker Chromosome In
- Cytogenetics Lecture 1: Introduction to Clinical Cytogenetics
- ISOCHROMOSOME NEOCENTROMERE 15Qter MOSAICISM Siri Huston, Yvette Rush, Tom Hempel, Ann Olney, Hope Chipman and Warren G
- Ring 22 Duplication/Deletion Mosaicism: Clinical, Cytogenetic, and Molecular Characterisation J Med Genet: First Published As 10.1136/Jmg.36.3.237 on 1 March 1999
- Cytogenetics: Nomenclature and Disease
- 3Disease Browser: a Web Server for Integrating 3D Genome and Disease
- Small Supernumerary Marker Chromosomes: a Legacy of Trisomy Rescue?
- Small Supernumerary Marker Chromosomes and Their Correlation with Specific Syndromes
- Supernumerary Marker of Chromosome 15 Associated With
- 22 Chromosome Chapter
- Genomic Rearrangements in Autism Spectrum Disorders: Identification of Novel Candidate Genes
- Diagnosis of Miscarriages by Molecular Karyotyping
- Cytogenetic Investigations in Four Canine Lymphomas
- Antenatal Cytogenetic Testing in Havana, Cuba
- 22 Inv Dup(15) and Inv Dup(22)
- Chromosome Abnormalities Reference
- A Small Supernumerary Marker Chromosome, Derived from Chromosome 22, Possibly Associated with Repeated Spontaneous Abortions
- A Unique Case of Female Pseudohermaphroditism with 21-Hydroxylase Deficiency and Small Supernumerary Marker Chromosome 7
- Angelman Syndrome, and Uniparental Disomy Resulting from Paternal Meiosis II Non-Disjunction S Roberts, F Maggouta, R Thompson, S Price, S Thomas
- Tetrasomy 9P
- Fetal Dna Chip Detection List 20160511