Ring chromosome 9 in a girl with developmental delay and dysmorphic features: Case report and review of the literature

Author:

Sibbesen Else la Cour1,Jespersgaard Cathrine1,Alosi Daniela1,Bisgaard Anne-Marie,Tümer Zeynep1

Affiliation:

1. Applied Human Molecular Genetics, Kennedy Center; Copenhagen University Hospital; Rigshospitalet, Glostrup; Denmark

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference40 articles.

1. Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA;Barbaro;Eur J Hum Genet,2009

2. Phenotypic variability in the chromosome 9 ring;Cavaliere;Acta Biomed Ateneo Parmense,1977

3. Prenatal diagnosis of mosaic ring chromosome 9;Chen;Prenat Diagn,2006

4. Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome;Christ;Am J Hum Genet,1999

5. Ring chromosome 9: Identification of a new case by G and C banding;Dipierri;Ann Genet,1982

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2. Ring chromosome formation by intra‐strand repairing of subtelomeric double stand breaks and clinico‐cytogenomic correlations for ring chromosome 9;American Journal of Medical Genetics Part A;2020-09-26

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