First small supernumerary ring chromosome carrying 10q euchromatin in a patient with mild phenotype characterized by molecular cytogenetic techniques and review of the literature | Citedby Results | Cytogenetic and Genome Research | Karger Publishers

Skip to Main Content

Skip Nav Destination

First small supernumerary ring chromosome carrying 10q euchromatin in a patient with mild phenotype characterized by molecular cytogenetic techniques and review of the literature

Cytogenet Genome Res (2005) 108 (4): 278–282.

This article has been cited by the following articles in journals that are participating in CrossRef Cited-by Linking.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(10) and monosomy 10 at amniocentesis in a fetus associated with perinatal growth restriction but no gross structural abnormalities

Chih-Ping Chen
Fang-Tzu Wu
Yen-Ting Pan
Peih-Shan Wu
Meng-Shan Lee
Chen-Wen Pan
Wayseen Wang

Taiwanese Journal of Obstetrics and Gynecology (2025) 64 (2): 339.

The first case of a small supernumerary marker chromosome derived from chromosome 10 in an adult woman with an apparently normal phenotype

Rosa Santacroce
Roberta Trunzo
Angelica Leccese
Angela Pansini
Mattia Gentile
Maurizio Margaglione

Systems Biology in Reproductive Medicine (2015) 61 (6): 398.

Clinical and molecular description of a fetus in prenatal diagnosis with a rare de novo ring 10 and deletions of 12.59Mb in 10p15.3–p14 and 4.22Mb in 10q26.3

G. Christopoulou
M. Tzetis
A.E. Konstantinidou
A. Tsezou
E. Kanavakis
S. Kitsiou-Tzeli
V. Velissariou

European Journal of Medical Genetics (2012) 55 (1): 75.

Identification and characterization of a complex pure mosaic of small supernumerary marker chromosomes involving 11p11.12 → q12.1 and 19p12 → q12 regions in a child featuring multiple congenital anomalies

Xiang Fei
Manlong Qi
Yanyan Zhao
Jesse Li‐Ling

American Journal of Medical Genetics Part A (2011) 155 (12): 3116.

Small supernumerary marker chromosome originating from chromosome 10 associated with an apparently normal phenotype

Pi‐Lin Sung
Sheng‐Ping Chang
Kuo‐Chang Wen
Chia‐Ming Chang
Ming‐Jie Yang
Lin‐Chao Chen
Kuan‐Chong Chao
Chi‐Ying F. Huang
Yueh‐Chun Li
Chyi‐Chyang Lin

American Journal of Medical Genetics Part A (2009) 149A (12): 2768.

Chromosome abnormalities without phenotypic consequences

Małgorzata Kowalczyk
Małgorzata Srebniak
Agnieszka Tomaszewska

Journal of Applied Genetics (2007) 48 (2): 157.