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1 . Academic Journal
High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissections
저자
by
Kathiravel, Ushanthine
;
Keyser, Britta
;
Hoffjan, Sabine
;
Kötting, Judith
;
Müller, Melanie
, et al.
소스
In
Molecular and Cellular Probes
April 2013 27(2):103-108
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7 . Academic Journal
Association of serotonin-1A and -2A receptor promoter polymorphisms with depressive symptoms, functional recovery, and pain in patients 6 months after lumbar disc surgery
저자
by
Lebe, Moritz
;
Hasenbring, Monika I.
;
Schmieder, Kirsten
;
Jetschke, Kathleen
;
Harders, Albrecht
, et al.
소스
In
Pain
March 2013 154(3):377-384
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7 . Academic Journal
Analysis of Rare APC Variants at the mRNA Level : Six Pathogenic Mutations and Literature Review
저자
by
Kaufmann, Astrid
;
Vogt, Stefanie
;
Uhlhaas, Siegfried
;
Stienen, Dietlinde
;
Kurth, Ingo
, et al.
소스
In
The Journal of Molecular Diagnostics
2009 11(2):131-139
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7 . Academic Journal
Severe demyelinating hypertrophic polyneuropathy caused by a de novo frameshift mutation within the intracellular domain of myelin protein zero ( MPZ/P0)
저자
by
Zschüntzsch, Jana
;
Dibaj, Payam
;
Pilgram, Sara
;
Kötting, Judith
;
Gerding, Wanda M.
, et al.
소스
In
Journal of the Neurological Sciences
2009 281(1):113-115
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7 . Academic Journal
Xp21/A Translocation: A Rarely Considered Genetic Cause for Manifesting Carriers of Duchenne Muscular Dystrophy
저자
by
Trippe, Heike
;
Wieczorek, Stefan
;
Kötting, Judith
;
Kress, Wolfram
;
Schara, Ulrike
.
소스
Neuropediatrics
. Oct 01, 2014 45(5):333-335
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7 . Academic Journal
Association of serotonin-1A and -2A receptor promoter polymorphisms with depressive symptoms, functional recovery, and pain in patients 6months after lumbar disc surgery
저자
by
Lebe, Moritz
;
Hasenbring, Monika I.
;
Schmieder, Kirsten
;
Jetschke, Kathleen
;
Harders, Albrecht
, et al.
소스
PAIN; Mar2013, Vol. 154 Issue 3, p377-384, 8p
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7 . Academic Journal
Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissections.
저자
by
Hoffjan, Sabine
;
Waldmüller, Stephan
;
Blankenfeldt, Wulf
;
Kötting, Judith
;
Gehle, Petra
, et al.
소스
European Journal of Human Genetics
. May2011, Vol. 19 Issue 5, p520-524. 5p. 2 Diagrams, 1 Chart, 1 Graph.
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7 . Academic Journal
UNUSUAL CHARCOT–MARIE–TOOTH PHENOTYPE DUE TO A MUTATION WITHIN THE INTRACELLULAR DOMAIN OF MYELIN PROTEIN ZERO
저자
by
SCHNEIDER-GOLD, CHRISTIANE
;
KÖTTING, JUDITH
;
EPPLEN, JÖRG T.
;
GOLD, RALF
;
GERDING, WANDA M.
.
소스
Muscle & Nerve
. Apr 01, 2010 41(4):550-554
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7 . Academic Journal
Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study.
저자
by
Campa, Daniele
;
Pardini, Barbara
;
Naccarati, Alessio
;
Vodickova, Ludmila
;
Novotny, Jan
, et al.
소스
BMC Gastroenterology
. 2010, Vol. 10, p112-117. 6p.
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7 . Academic Journal
Expanded HSAN4 phenotype associated with two novel mutations in NTRK1
저자
by
Wieczorek, Stefan
;
Bergström, Jonas
;
Sääf, Maria
;
Kötting, Judith
;
Iwarsson, Erik
.
소스
Neuromuscular Disorders
. Aug2008, Vol. 18 Issue 8, p681-684. 4p.
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