Intrachromosomal insertion mimicking a pericentric inversion: Molecular cytogenetic characterization of a three break rearrangement of chromosome 20
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference31 articles.
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2. Constitutional deletion of chromosome 20q in two patients affected with albright hereditary osteodystrophy
3. Adenomatous polyposis coli and a cytogenetic deletion of chromosome 5 resulting from a maternal intrachromosomal insertion.
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5. A familial balanced inverted insertion ins(15)(q15q13q11.2) producing Prader-Willi syndrome, Angelman syndrome and duplication of 15q11.2-q13 in a single family: Importance of differentiation from a paracentric inversion
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1. Genome-wide noninvasive prenatal screening for carriers of balanced reciprocal translocations;Genetics in Medicine;2020-12
2. A 105 kb interstitial insertion in the Xq27.1 palindrome from pseudoautosomal region PAR1 causes a novel X-linked recessive compound phenotype;Journal of Translational Medicine;2019-04-29
3. Two familial intrachromosomal insertions with maternal dup(6)(p22.3p25.3) or dup(2)(q24.2q32.1) in recombinant offspring;Clinical Dysmorphology;2017-10
4. PGD for a carrier of an intrachromosomal insertion using aCGH;Systems Biology in Reproductive Medicine;2014-09-23
5. The variable phenotypes of KCNQ-related epilepsy;Epilepsia;2014-07-22
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