Pages that link to "Q36719179"
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The following pages link to Mechanisms and consequences of small supernumerary marker chromosomes: from Barbara McClintock to modern genetic-counseling issues (Q36719179):
Displaying 34 items.
- Centromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogenetics (Q30512201) (← links)
- Molecular cytogenetics and cytogenomics of brain diseases (Q33464340) (← links)
- Interstitial deletion of proximal 8q including part of the centromere from unbalanced segregation of a paternal deletion/marker karyotype with neocentromere formation at 8p22. (Q34724909) (← links)
- Small supernumerary marker chromosomes and uniparental disomy have a story to tell (Q35441030) (← links)
- Gain of FAM123B and ARHGEF9 in an Obese Man with Intellectual Disability, Congenital Heart Defects and Multiple Supernumerary Ring Chromosomes (Q36600637) (← links)
- Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II Errors (Q36634982) (← links)
- Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridization (Q36645381) (← links)
- Meiotic and mitotic behaviour of a ring/deleted chromosome 22 in human embryos determined by preimplantation genetic diagnosis for a maternal carrier (Q37087137) (← links)
- DNA probe pooling for rapid delineation of chromosomal breakpoints (Q37212268) (← links)
- Human Ring Chromosomes - New Insights for their Clinical Significance (Q37328960) (← links)
- Handling small supernumerary marker chromosomes in prenatal diagnostics (Q37478688) (← links)
- Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances (Q37857750) (← links)
- Normal prenatal ultrasound findings in a case with de novo mosaic small supernumerary marker chromosome 18--how to counsel? (Q37863100) (← links)
- Tetrasomy 9p mosaicism associated with a normal phenotype in two cases (Q38001254) (← links)
- A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity (Q38039304) (← links)
- Detecting genomic imbalances in prenatal diagnosis: main hurdles and recent advances (Q38089061) (← links)
- Molecular cytogenetic characterization of two Turner syndrome patients with mosaic ring X chromosome (Q41011777) (← links)
- Interstitial 4q Deletion and Isodicentric Y-Chromosome in a Patient with Dysmorphic Features. (Q41960929) (← links)
- Somatic mosaicism in cases with small supernumerary marker chromosomes (Q42040542) (← links)
- Clinical impact of proximal autosomal imbalances (Q42633782) (← links)
- Design and validation of a pericentromeric BAC clone set aimed at improving diagnosis and phenotype prediction of supernumerary marker chromosomes (Q42917226) (← links)
- Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective study. (Q44292036) (← links)
- Ring chromosomes: from formation to clinical potential. (Q48089215) (← links)
- Novel phenotype of 5p13.3-q11.2 duplication resulting from supernumerary marker chromosome 5: implications for management and genetic counseling. (Q52620494) (← links)
- A Marfan syndrome-like phenotype caused by a neocentromeric supernumerary ring chromosome 15. (Q52675805) (← links)
- Characterizing small supernumerary marker chromosomes with combination of multiple techniques. (Q54336681) (← links)
- Genomic characterization of prenatally detected chromosomal structural abnormalities using oligonucleotide array comparative genomic hybridization. (Q55603052) (← links)
- Karyotype/phenotype correlation in partial trisomies of the long arm of chromosome 16: Case report and review of literature (Q57790305) (← links)
- Mechanism and Genotype-Phenotype Correlation of Two Proximal 6q Deletions Characterized Using mBAND, FISH, Array CGH, and DNA Sequencing (Q58459194) (← links)
- Mosaic partial trisomy 19p12-q13.11 due to a small supernumerary marker chromosome: A locus associated with Asperger syndrome? (Q58488483) (← links)
- Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 21 (Q82343338) (← links)
- Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18 (Q84738231) (← links)
- Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres? (Q85216389) (← links)
- The Identification and Analysis of mRNA-lncRNA-miRNA Cliques From the Integrative Network of Ovarian Cancer (Q93186457) (← links)