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Clinical and mutational spectrum of Mowat-Wilson syndrome.
Eur J Med Genet. 2005 Apr-Jun;48(2):97-111. doi: 10.1016/j.ejmg.2005.01.003. Epub 2005 Feb 25.
Eur J Med Genet. 2005.
PMID: 16053902
Hyperphosphatasia-mental retardation syndrome due to PIGV mutations: expanded clinical spectrum.
Horn D, Krawitz P, Mannhardt A, Korenke GC, Meinecke P.
Horn D, et al. Among authors: mannhardt a.
Am J Med Genet A. 2011 Aug;155A(8):1917-22. doi: 10.1002/ajmg.a.34102. Epub 2011 Jul 7.
Am J Med Genet A. 2011.
PMID: 21739589
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Mosaic and complete tetraploidy in live-born infants: two new patients and review of the literature.
Stefanova I, Jenderny J, Kaminsky E, Mannhardt A, Meinecke P, Grozdanova L, Gillessen-Kaesbach G.
Stefanova I, et al. Among authors: mannhardt a.
Clin Dysmorphol. 2010 Jul;19(3):123-127. doi: 10.1097/MCD.0b013e3283353877.
Clin Dysmorphol. 2010.
PMID: 20305547
Review.
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"Double reflection": a practical approach to teach patient-doctor communication in oncology.
Mannhardt AK, Ogbonnaya L, Gieseler F.
Mannhardt AK, et al.
Oncologist. 2013;18(9):1058. doi: 10.1634/theoncologist.2013-0125.
Oncologist. 2013.
PMID: 24062424
Free PMC article.
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