Pigmentary dysplasias in long survivors with mosaic trisomy 18: report of two cases
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1991.tb02988.x/fullpdf
Reference29 articles.
1. Tetraploidy and 18-trisomy in a six-year-old triple mosaic boy;Atnip;Cytogenetics,1971
2. Trisomy 18 mosaicism: clues to the diagnosis;Bass;Clin. Genet.,1982
3. A mildly retarded woman with 46XX/47 XX + 18 mosaicism;Bensen;Am. J. Med. Genet.,1985
4. Parental mosaicism in trisomy 18;Beratis;Pediatrics,1972
5. Survival in trisomy 18. Life tables for use in genetic counseling and clinical paediatrics;Carter;Clin. Genet.,1985
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1. Mosaic Disorders of Pigmentation;Harper's Textbook of Pediatric Dermatology;2019-11-20
2. Pigmentary mosaicism: a review of original literature and recommendations for future handling;Orphanet Journal of Rare Diseases;2018-03-05
3. Trisomy 18 mosaicism with complete peripheral lymphocyte trisomy and normal intelligence;Clinical Genetics;2008-06-28
4. Phenotypic spectrum of mosaic trisomy 18: Two new patients, a literature review, and counseling issues;American Journal of Medical Genetics Part A;2007
5. Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes;British Journal of Dermatology;2004-08
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