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Title
Myhre syndrome
Authors
Keywords
-
Journal
CLINICAL GENETICS
Volume 85, Issue 6, Pages 503-513
Publisher
Wiley
Online
2014-03-03
DOI
10.1111/cge.12365
References
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Related references
Note: Only part of the references are listed.- Myhre and LAPS syndromes: clinical and molecular review of 32 patients
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- (2012) Carine Le Goff et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
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- Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome
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- (2010) D. Garcia-Cruz et al. CLINICAL GENETICS
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- (2010) Michael A. Soljak et al. CLINICAL GENETICS
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- (2010) Selma A. Myhre et al. CLINICAL GENETICS
- Mutations in Fibrillin-1 Cause Congenital Scleroderma: Stiff Skin Syndrome
- (2010) B. L. Loeys et al. Science Translational Medicine
- LAPS syndrome and Myhre syndrome: Two disorders or one?
- (2009) Noralane M. Lindor AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- The fifth female patient with Myhre syndrome: further delineation
- (2009) Luis E. Becerra-Solano et al. CLINICAL DYSMORPHOLOGY
- ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-β bioavailability regulation
- (2008) Carine Le Goff et al. NATURE GENETICS
- How the Smads regulate transcription
- (2007) Sarah Ross et al. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
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