Grouping of Multiple-Lentigines/LEOPARD and Noonan Syndromes on the PTPN11 Gene

Multiple-lentigines (ML)/LEOPARD (multiple lentigines, electrocardiographic-conduction abnormalities, ocular hypertelorism, pulmonary stenosis, abnormal genitalia, retardation of growth, and sensorineural deafness) syndrome is an autosomal dominant condition—characterized by lentigines and café au l...

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Bibliografische gegevens
Hoofdauteurs: Digilio, Maria Cristina, Conti, Emanuela, Sarkozy, Anna, Mingarelli, Rita, Dottorini, Tania, Marino, Bruno, Pizzuti, Antonio, Dallapiccola, Bruno
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: The American Society of Human Genetics 2002
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC379170/
https://ncbi.nlm.nih.gov/pubmed/12058348
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