Pages that link to "Q39789768"
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The following pages link to Characterization of a recurrent 15q24 microdeletion syndrome. (Q39789768):
Displaying 50 items.
- Mapping and sequencing of structural variation from eight human genomes (Q22122215) (← links)
- DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources (Q24644530) (← links)
- Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication (Q24646722) (← links)
- Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes (Q24655755) (← links)
- Structural variation of chromosomes in autism spectrum disorder (Q24656970) (← links)
- Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals (Q27345314) (← links)
- Mammalian sex determination—insights from humans and mice (Q27691819) (← links)
- Further clinical and molecular delineation of the 15q24 microdeletion syndrome (Q28732710) (← links)
- Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size (Q29544005) (← links)
- The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype (Q30477238) (← links)
- Molecular cytogenetics and cytogenomics of brain diseases (Q33464340) (← links)
- Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans (Q33515390) (← links)
- Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genes (Q33620872) (← links)
- A chromosomal microdeletion of 15q in a female patient with epilepsy, ID, and autism spectrum disorder: a case report (Q33760937) (← links)
- Inversion variants in the human genome: role in disease and genome architecture (Q33762256) (← links)
- From microscopes to microarrays: dissecting recurrent chromosomal rearrangements (Q33805828) (← links)
- Evolution in health and medicine Sackler colloquium: Genomic disorders: a window into human gene and genome evolution (Q33844453) (← links)
- The functional impact of structural variation in humans (Q33847296) (← links)
- Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21. (Q33851454) (← links)
- Genomics, intellectual disability, and autism (Q33937230) (← links)
- A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region (Q34009775) (← links)
- Copy number variation in human health, disease, and evolution (Q34019142) (← links)
- Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk (Q34053455) (← links)
- Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach (Q34089144) (← links)
- New Technologies for the Identification of Novel Genetic Markers of Disorders of Sex Development (DSD) (Q34168852) (← links)
- Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes (Q34452268) (← links)
- Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability (Q34572542) (← links)
- Parental imbalances involving chromosomes 15q and 22q may predispose to the formation of de novo pathogenic microdeletions and microduplications in the offspring (Q34618442) (← links)
- Phenotypic manifestations of copy number variation in chromosome 16p13.11. (Q34705135) (← links)
- Disorders caused by chromosome abnormalities (Q34775497) (← links)
- Genome destabilization by homologous recombination in the germ line (Q34778117) (← links)
- Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture (Q34990719) (← links)
- Chromosome 15q24 microdeletion syndrome (Q35744734) (← links)
- The genetics of microdeletion and microduplication syndromes: an update. (Q35765523) (← links)
- Ancient Haplotypes at the 15q24.2 Microdeletion Region Are Linked to Brain Expression of MAN2C1 and Children's Intelligence (Q36063978) (← links)
- Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome (Q36091184) (← links)
- Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders (Q36611957) (← links)
- Genomic rearrangements and sporadic disease (Q36863512) (← links)
- Inducing segmental aneuploid mosaicism in the mouse through targeted asymmetric sister chromatid event of recombination (Q36873757) (← links)
- Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping (Q36893488) (← links)
- The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome (Q36943643) (← links)
- Oligonucleotide arrays for high-resolution analysis of copy number alteration in mental retardation/multiple congenital anomalies (Q36943647) (← links)
- Mechanisms for human genomic rearrangements (Q36975128) (← links)
- Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant. (Q37135729) (← links)
- Population analysis of large copy number variants and hotspots of human genetic disease (Q37156109) (← links)
- Novel microdeletion syndromes detected by chromosome microarrays (Q37177145) (← links)
- Genomic disorders ten years on. (Q37198442) (← links)
- Characterization of six human disease-associated inversion polymorphisms (Q37239862) (← links)
- Emerging themes and new challenges in defining the role of structural variation in human disease (Q37287518) (← links)
- Genomic microarrays in mental retardation: a practical workflow for diagnostic applications (Q37351805) (← links)