Mapping breakpoints of a familial chromosome insertion (18,7) (q22.1; q36.2q21.11) to DPP6 and CACNA2D1 genes in an azoospermic male

References

Page 1

	Year	Citations
SOAP: short oligonucleotide alignment program Ruiqiang Li, Yingrui Li, Karsten Kristiansen, Bioinformatics	2008	3.6K
A gene atlas of the mouse and human protein-encoding transcriptomes Andrew I. Su, Tim Wiltshire, Serge Batalov, Proceedings of the National Academy of Sciences EngineeringGeneticsTranscriptomics TechnologyGene CharacterizationMolecular Genetics	2004	3.5K
Structural Variation of Chromosomes in Autism Spectrum Disorder Christian R. Marshall, Abdul Noor, John B. Vincent, The American Journal of Human Genetics ChromatinStructural VariationSyndromic AutismGeneticsMolecular Biology	2008	1.8K
R-spondins function as ligands of the orphan receptors LGR4 and LGR5 to regulate Wnt/β-catenin signaling Kendra S. Carmon, Xing Gong, Qiushi Lin, Proceedings of the National Academy of Sciences Stem Cell GrowthMolecular RegulationCellular PhysiologyTissue DevelopmentCell Regulation	2011	847
R-spondin1 is essential in sex determination, skin differentiation and malignancy P. Parma, Orietta Radi, Valérie Vidal, Nature Genetics GeneticsMolecular GeneticsSkin DifferentiationDermatologyExperimental Dermatology	2006	766
Mechanisms for human genomic rearrangements Wenli Gu, Feng Zhang, James R. Lupski PathoGenetics	2008	718
EAA/EMQN best practice guidelines for molecular diagnosis of y‐chromosomal microdeletions. State of the art 2004 Manuela Simoni, Egbert Bakker, Csilla Krausz International Journal of Andrology	2004	483
Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding. P. A. Jacobs, C.E. Browne, N. Gregson, Journal of Medical Genetics Developmental AnomalyModerate LevelsNeonatologyCytogeneticsMedicine	1992	416
Human Chromosome 7: DNA Sequence and Biology Stephen W. Scherer, Joseph Cheung, Jeffrey R. MacDonald, Science DnaCytogeneticsGeneticsMolecular BiologyHigher Order Description	2003	214
Insertional translocation detected using FISH confirmation of array‐comparative genomic hybridization (aCGH) results Sung‐Hae Kang, Chad A. Shaw, Zhishuo Ou, American Journal of Medical Genetics Part A CytogeneticsGeneticsComplex ItPathologyGenomics	2010	166

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