LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD.

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LEOPARD Syndrome: Clinical Features and Gene Mutations.A case of congenital hypertrophic cardiomyopathy.The Role of Insulin-Like Growth Factor 1 in the Progression of Age-Related Hearing Loss.

P2860

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P2860

LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD.

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http://www.wikidata.org/entity/Q42089211

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2011 nî lūn-bûn

@nan

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

2011年论文

@zh

2011年论文

@zh-cn

name

LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD.

@en

LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD.

@nl

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Item

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LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD.

@en

LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD.

@nl

prefLabel

LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD.

@en

LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD.

@nl

P1476

LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD.

@en

P2093

Hee Jung Kim

http://www.w3.org/2001/XMLSchema#string

Jihyun Kim

http://www.w3.org/2001/XMLSchema#string

Kyung-A Lee

http://www.w3.org/2001/XMLSchema#string

Mi Ri Kim

http://www.w3.org/2001/XMLSchema#string

Min-Geol Lee

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P2860

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

Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.

Acute myelomonocytic leukemia in a boy with LEOPARD syndrome (PTPN11 gene mutation positive)

Multiple lentigenes syndrome

Multiple granular cell tumors are an associated feature of LEOPARD syndrome caused by mutation in PTPN11

Intense pulsed light for the treatment of lentigines in LEOPARD syndrome.

Clinical and molecular analysis of 30 patients with multiple lentigines LEOPARD syndrome.

Correlation between PTPN11 gene mutations and congenital heart defects in Noonan and LEOPARD syndromes.

Common acute lymphoblastic leukemia in a girl with genetically confirmed LEOPARD syndrome.

Malignant melanoma in a woman with LEOPARD syndrome: identification of a germline PTPN11 mutation and a somatic BRAF mutation.

P304

232-235

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P31

scholarly article

case report

P356

10.5021/AD.2011.23.2.232

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

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2011-05-27T00:00:00Z

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51484236

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21747628

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P932

3130872

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LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD.

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P2860

P2860

LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD.

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type

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932