Suchergebnisse - Zschocke, Johannes
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Clinical utility gene card for: Phenylketonuria von Zschocke, Johannes, Haverkamp, Thomas, Møller, Lisbeth Birk
Veröffentlicht 2012Text -
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Oral manifestations of Ehlers‐Danlos syndromes von Lepperdinger, Ulrike, Zschocke, Johannes, Kapferer‐Seebacher, Ines
Veröffentlicht 2021Text -
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Maternal ABCA1 genotype is associated with severity of Smith–Lemli–Opitz syndrome and with viability of patients homozygous for null mutations von Lanthaler, Barbara, Steichen-Gersdorf, Elisabeth, Kollerits, Barbara, Zschocke, Johannes, Witsch-Baumgartner, Martina
Veröffentlicht 2013Text -
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Erratum: Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD) von Morava, Eva, Baumgartner, Matthias, Patterson, Marc, Rahman, Shamima, Zschocke, Johannes, Peters, Verena
Veröffentlicht 2017Text -
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Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutations von Tavasoli, Ali Reza, Parvaneh, Nima, Ashrafi, Mahmoud Reza, Rezaei, Zahra, Zschocke, Johannes, Rostami, Parastoo
Veröffentlicht 2018Text -
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An exceptional Albanian family with seven children presenting with dysmorphic features and mental retardation: maternal phenylketonuria von Knerr, Ina, Zschocke, Johannes, Schellmoser, Stefan, Topf, Hans G, Weigel, Corina, Dötsch, Jörg, Rascher, Wolfgang
Veröffentlicht 2005Text -
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