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Hyperphosphatasia-mental retardation syndrome due to PIGV mutations: expanded clinical spectrum.
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
Clinical and mutational spectrum of Mowat-Wilson syndrome.
Zweier C, Thiel CT, Dufke A, Crow YJ, Meinecke P, Suri M, Ala-Mello S, Beemer F, Bernasconi S, Bianchi P, Bier A, Devriendt K, Dimitrov B, Firth H, Gallagher RC, Garavelli L, Gillessen-Kaesbach G, Hudgins L, Kääriäinen H, Karstens S, Krantz I, Mannhardt A, Medne L, Mücke J, Kibaek M, Krogh LN, Peippo M, Rittinger O, Schulz S, Schelley SL, Temple IK, Dennis NR, Van der Knaap MS, Wheeler P, Yerushalmi B, Zenker M, Seidel H, Lachmeijer A, Prescott T, Kraus C, Lowry RB, Rauch A.
Zweier C, et al. Among authors: mannhardt a.
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
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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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