Marker chromosome
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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