Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB-Reference-Cited by-同舟云学术

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Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB

Published:2014-03 Issue:1 Volume:4 Page:
ISSN:2211-8039
Container-title:BioMedicine
language:en
Short-container-title:BioMed

Author:

Chang Yu-Tzu,Wang Chung-Hsing,Chou I-Ching,Lin Wei-De,Chee Siew-Yin,Kuo Huang-Tsung,Tsai Fuu-Jen

Publisher

China Medical University

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference20 articles.

1. Moortgat S, Verellen-Dumoulin C, Maystadt I, Parmentier B, Grisart B, Hennecker JL, et al. Developmental delay and facial dysmorphism in a child with an 8.9 Mb de novo interstitial deletion of 3q25.1-q25.32: Genotype-phenotype correlations of chromosome 3q25 deletion syndrome. Eur J Med Genet 2011; 54: 177–80.

2. Franceschini P, Cirillo Silengo M, Davi G, Bianco R, Biagioli M. Interstitial deletion of the long arm of chromosome 3 in a patient with mental retardation and congenital anomalies. Hum Genet 1983;64:97.

3. Martsolf JT, Ray M. Interstitial deletion of the long arm of chromosome 3. Ann Genet 1983; 26: 98–99.

4. Al-Awadi SA, Naguib KK, Farag TI, Teebi AS, Cuschieri A, Al-Othman SA, et al. Complex translocation involving chromosomes Y, 1, and 3 resulting in deletion of segment 3q23-q25. J Med Genet 1986;23:91–92.

5. Alvarado M, Bocian M, Walker AP. Interstitial deletion of the long arm of chromosome 3: case report, review, and definition of a phenotype. Am J Med Genet 1987; 27: 781–86.

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