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/vufind/Search/Results?lookfor=%22Megarbane%2C+Andre%22&type=Person&page=9
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PubPharm (489)
81
Genome sequencing unveils mutational landscape of the familial Mediterranean fever : Potential implications of IL33/ST2 signalling
enthalten in:
Journal of Cellular and Molecular Medicine
| 2020
von
Umar, M.
|
Megarbane, A.
|
Shan, J.
| +8
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82
Further Delineation of the TRAPPC6B Disorder : Report on a New Family and Review
enthalten in:
Journal of pediatric genetics
| 2019
von
Nair, P.
|
El-Bazzal, L.
|
Mansour, H.
| +6
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83
Methylomic profiling in trisomy 21 identifies cognition- and Alzheimer's disease-related dysregulation
enthalten in:
Clinical epigenetics
| 2019
von
Haertle, L.
|
Müller, T.
|
Lardenoije, R.
| +19
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84
Methylomic profiling in trisomy 21 identifies cognition- and Alzheimer’s disease-related dysregulation
enthalten in:
Clinical epigenetics
| 2019
von
Haertle, L.
|
Müller, T.
|
Lardenoije, R.
| +19
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85
A novel PDE6D mutation in a patient with Joubert syndrome type 22 (JBTS22)
enthalten in:
European journal of medical genetics
| 2019
von
Mégarbané, A.
|
Hmaimess, G.
|
Bizzari, S.
| +5
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86
The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries
enthalten in:
Human mutation
| 2019
von
Laitman, Y.
|
Friebel, T.
|
Yannoukakos, D.
| +33
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87
Mitochondrial DNA control region variation in Lebanon, Jordan, and Bahrain
enthalten in:
Forensic science international. Genetics
| 2019
von
Zimmermann, B.
|
Sturk-Andreaggi, K.
|
Huber, N.
| +11
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88
A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs)
enthalten in:
Annals of neurology
| 2019
von
Pareyson, D.
|
Stojkovic, T.
|
Reilly, M.
| +39
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89
Loss of Cajal bodies in motor neurons from patients with novel mutations in VRK1
enthalten in:
Human molecular genetics
| 2019
von
El-Bazzal, L.
|
Rihan, K.
|
Bernard-Marissal, N.
| +11
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90
Report of a Second Lebanese Family with Basel-Vanagaite-Smirin-Yosef Syndrome : Possible Founder Mutation
enthalten in:
Molecular syndromology
| 2019
von
Nair, P.
|
Sabbagh, S.
|
Bizzari, S.
| +6
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