Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis.

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Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis.

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2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis.

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Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis.

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Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis.

@en

Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis.

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Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis.

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Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis.

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P1476

Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis.

@en

P2093

A Medlar

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H Stanescu

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L Nibali

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N Donos

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R Kleta

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U Darbar

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P2860

Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome

A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1

Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations

Human and mouse amelogenin gene loci are on the sex chromosomes

Evidence of genetic heterogeneity for hereditary gingival fibromatosis.

Genetic studies of craniofacial anomalies: clinical implications and applications

Hereditary gingival fibromatosis: a systematic review.

Characterization of fibroblasts with Son of Sevenless-1 mutation

GWAS or Gee Whiz, PSAS or Pshaw: elucidating the biologic and clinical significance of genetic variation in cardiovascular disease.

Identification of genetic markers associated with high-density lipoprotein-cholesterol by genome-wide screening in a Japanese population: the Suita study.

P304

100-105

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scholarly article

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10.1111/J.1601-0825.2012.01965.X

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2012-07-31T00:00:00Z

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22849749

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