Grouping of multiple-lentigines/LEOPARD and Noonan syndromes on the PTPN11 gene

American Journal of Human Genetics

Volumn 71, Issue 2, 2002, Pages 389-394

  Digilio, Maria Cristina ^a   Conti, Emanuela ^b,c   Sarkozy, Anna ^b,c   Mingarelli, Rita ^b   Dottorini, Tania ^b   Marino, Bruno ^d   Pizzuti, Antonio ^b,c   Dallapiccola, Bruno ^b,c  

^a BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^b CASA SOLLIEVO DELLA SOFFERENZA HOSPITAL   (Italy)

^c Institute of Medical Genetics   (Italy)

^d SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN TYROSINE PHOSPHATASE;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHILD; CHROMOSOME 12Q; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; FEMALE; GENE; HUMAN; LENTIGO; LEOPARD SYNDROME; MALE; MALFORMATION SYNDROME; MISSENSE MUTATION; NOONAN SYNDROME; PRIORITY JOURNAL; PTPN11 GENE; SINGLE STRAND CONFORMATION POLYMORPHISM; SYNDROME DELINEATION;

PANTHERA PARDUS;

EID: 0036074033     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/341528     Document Type: Article

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