Exclusion of Candidate Genes and Loci for Multiple Lentigines Syndrome
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference21 articles.
1. Noonan syndrome with cafe-au-lait spots and multiple lentigines syndrome are not linked to the neurofibromatosis type 1 locus;Ahlbom;Clin Genet,1995
2. Pigmentary anomalies in the multiple lentigines syndrome: Is it distinct from LEOPARD syndrome?;Arnsmeier;Pediatr Dermatol,1996
3. Unifying link between Noonan's and Leopard syndromes?;Blieden;Pediatr Cardiol,1983
4. Multiple lentigines syndrome. a comparison of normal skin and lentiginous skin by electron microscopy and immunohistochemical staining;Choi;J Dermatol,1998
5. Multiple lentigines syndrome (LEOPARD syndrome or progressive cardiomyopathic lentiginosis);Coppin;J Med Genet,1997
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1. SASH1 S519N Variant Links Skin Hyperpigmentation and Premature Hair Graying to Dysfunction of Melanocyte Lineage;Journal of Investigative Dermatology;2024-06
2. SASH1 Is Involved in an Autosomal Dominant Lentiginous Phenotype;Journal of Investigative Dermatology;2015-12
3. The lentiginoses: cutaneous markers of systemic disease and a window to new aspects of tumourigenesis;Journal of Medical Genetics;2005-06-15
4. Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11;Journal of Human Genetics;2004-12-10
5. Genetic heterogeneity in the multiple lentigines/LEOPARD/Noonan syndromes;American Journal of Medical Genetics;2004
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