Rare interstitial deletion (2)(p11.2p13) in a child with pericentric inversion (2)(p11.2q13) of paternal origin
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference17 articles.
1. Study on segregation and risk for abnormal offspring in carriers of pericentric inversion of the (p11←q13) segment of chromosome 2
2. The significance of pericentric inversions of chromosome 2
3. Tiny interstitial duplication of proximal 7q in association with a maternal paracentric inversion
4. Interstitial duplication/deletion owing to unequal crossing-over in association with pericentric inversion.
5. A cytogenetic survey of 11,680 newborn infants
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1. Prenatal Diagnosis of Chromosomal Abnormalities through Chorionic Villus Sampling and Amniocentesis;Genetic Disorders and the Fetus;2021-04-20
2. Recombinant Chromosomes Resulting From Parental Pericentric Inversions—Two New Cases and a Review of the Literature;Frontiers in Genetics;2019-11-14
3. Cytogenetic, Molecular, and Phenotypic Characterization of a Patient with de novo Derivative Chromosome 18 and Review of the Literature;Cytogenetic and Genome Research;2019
4. Rare interstitial deletion of chromosome 2p11.2p12. Report of a new patient with developmental delay and unusual clinical features;European Journal of Medical Genetics;2016-01
5. Prenatal Diagnosis of Chromosomal Abnormalities through Chorionic Villus Sampling and Amniocentesis;Genetic Disorders and the Fetus;2015-11-23
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