Microdeletion Syndromes Detected by FISH – 73 Positive from 374 Cases
Author:
Affiliation:
1. Department of Assisted Reproduction and Genetics, Jaslok Hospital and Research Centre, Mumbai 400 026, Maharashtra, India E-mail: geneticsjaslok@gmail.com, prochi_madon@yahoo.com
Publisher
Kamla Raj Enterprises
Subject
Genetics (clinical),Genetics
Link
https://www.tandfonline.com/doi/pdf/10.1080/09723757.2010.11886080
Reference4 articles.
1. Baraitser M, Winter RM 1996.Color Atlas of Congenital Malformation Syndromes. Spain: Times Mirror International Publishers Limited.
2. Jorde LB, Carey JC, Bamshad MJ, White RL 2000.Medical Genetics. USA: Mosby, Inc.
3. Shaffer LG, Bejjani BA, Torchia B, Kirkpatrick S, Croppinger J, Ballif BC 2007. The identification of microdeletion syndromes and other chromosome abnormalities: cytogenetic methods of the past, new technologies for the future.Am J Med Genet C Semin Med Genet, 145C(4): 335–345.
4. Vogels A, Fryns JP 2004. Microdeletions and Molecular Genetics.Atlas Genet Cytogenet Oncol Haematol, February 2004 http://AtlasGeneticsOncology.org/Educ/MicrodeletionID30059ES.html (Accessed on 09. 01. 2010).
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