标题
Myhre syndrome: Clinical features and restrictive cardiopulmonary complications
作者
关键词
-
出版物
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume 167, Issue 12, Pages 2893-2901
出版商
Wiley
发表日期
2015-09-30
DOI
10.1002/ajmg.a.37273
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Myhre-LAPs syndrome and intubation related airway stenosis: keys to diagnosis and critical therapeutic interventions
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- Myhre syndrome with facial paralysis and branch pulmonary stenosis
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- NovelSMAD4mutation causing Myhre syndrome
- (2014) Viviana Caputo et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Myhre syndrome
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- Myhre syndrome: a rare craniofacial disorder
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- Myhre and LAPS syndromes: clinical and molecular review of 32 patients
- (2014) Caroline Michot et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- SMAD4 mutations causing Myhre syndrome result in disorganization of extracellular matrix improved by losartan
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- Bilateral Otospongiosis and a Unilateral Vestibular Schwannoma in a Patient With Myhre Syndrome
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- Recurrent Pericarditis in Myhre Syndrome
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- A Restricted Spectrum of Mutations in the SMAD4 Tumor-Suppressor Gene Underlies Myhre Syndrome
- (2012) Viviana Caputo et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mutations of SMAD4 account for both LAPS and Myhre syndromes
- (2012) Noralane M. Lindor et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- First case of a Japanese girl with Myhre syndrome due to a heterozygousSMAD4mutation
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- From tall to short: The role of TGFβ signaling in growth and its disorders
- (2012) Carine Le Goff et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
- Retinal involvement in two unrelated patients with Myhre syndrome
- (2012) Essam Al Ageeli et al. European Journal of Medical Genetics
- Smad4 disruption accelerates keratinocyte reepithelialization in murine cutaneous wound repair
- (2012) Leilei Yang et al. HISTOCHEMISTRY AND CELL BIOLOGY
- Myhre syndrome with ataxia and cerebellar atrophy
- (2011) Ruxandra Bachmann-Gagescu et al. CLINICAL DYSMORPHOLOGY
- Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome
- (2011) Carine Le Goff et al. NATURE GENETICS
- A new growth deficiency syndrome
- (2010) Selma A. Myhre et al. CLINICAL GENETICS
- LAPS syndrome and Myhre syndrome: Two disorders or one?
- (2009) Noralane M. Lindor AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Atrial fibrosis and atrial fibrillation: The role of the TGF-β1 signaling pathway
- (2009) Felix Gramley et al. INTERNATIONAL JOURNAL OF CARDIOLOGY
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