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Oppelt, Peter; Binder, Helge; Birraux, Jacques; Brucker, Sara; Dingeldein, Irene; Draths, Ruth; Eckoldt, Felicitas; Füllers, Ulrich; Hiort, Olaf; Hoffmann, Dorit; Hoopmann, Markus; Hucke, Jürgen; Korell, Matthias; Kühnert, Maritta; Ludwikowski, Barbara; Mentzel, Hans-Joachim; Mon OʼDey, Dan; Rall, Katharina; Riccabona, Michael; Rimbach, Stefan; ... (2021). Diagnosis and Therapy of Female Genital Malformations (Part 1). Guideline of the DGGG, OEGGG and SGGG (S2k Level, AWMF Registry Number 015/052, May 2019). Geburtshilfe und Frauenheilkunde, 81(12), pp. 1307-1328. Thieme 10.1055/a-1471-4781
Oppelt, Peter; Binder, Helge; Birraux, Jacques; Brucker, Sara; Dingeldein, Irene; Draths, Ruth; Eckoldt, Felicitas; Füllers, Ulrich; Hiort, Olaf; Hoffmann, Dorit; Hoopmann, Markus; Hucke, Jürgen; Korell, Matthias; Kühnert, Maritta; Ludwikowski, Barbara; Mentzel, Hans-Joachim; Mon OʼDey, Dan; Rall, Katharina; Riccabona, Michael; Rimbach, Stefan; ... (2021). Diagnosis and Therapy of Female Genital Malformations (Part 2). Guideline of the DGGG, OEGGG and SGGG (S2k Level, AWMF Registry Number 015/052, May 2019). Geburtshilfe und Frauenheilkunde, 81(12), pp. 1329-1347. Thieme 10.1055/a-1471-4988
Boettcher, Claudia; Utsch, Boris; Galler, Angela; Grasemann, Corinna; Borkenstein, Martin; Denzer, Christian; Heidtmann, Bettina; Tittel, Sascha R; Holl, Reinhard W (2020). Estimated Glomerular Filtration Rates Calculated by New and Old Equations in Children and Adolescents With Type 1 Diabetes-What to Do With the Results? Frontiers in endocrinology, 11(52), p. 52. Frontiers Research Foundation 10.3389/fendo.2020.00052
Hoefele, Julia; Wolf, Matthias T F; O'Toole, John F; Otto, Edgar A; Schultheiss, Ulla; Dêschenes, Georges; Attanasio, Massimo; Utsch, Boris; Antignac, Corinne; Hildebrandt, Friedhelm (2007). Evidence of oligogenic inheritance in nephronophthisis. Journal of the American Society of Nephrology, 18(10), pp. 2789-95. Hagerstown, Md.: Lippincott Williams & Wilkins 10.1681/ASN.2007020243
Utsch, Boris; McCabe, Colleen D; Galbraith, Kenneth; Gonzalez, Ricardo; Born, Mark; Dötsch, Jörg; Ludwig, Michael; Reutter, Heiko; Innis, Jeffrey W (2007). Molecular characterization of HOXA13 polyalanine expansion proteins in hand-foot-genital syndrome. American journal of medical genetics. Part A, 143A(24), pp. 3161-8. Hoboken, N.J.: Wiley-Liss 10.1002/ajmg.a.31967
Helou, Juliana; Otto, Edgar A; Attanasio, Massimo; Allen, Susan J; Parisi, Melissa A; Glass, Ian; Utsch, Boris; Hashmi, Seema; Fazzi, Elisa; Omran, Heymut; O'Toole, John F; Sayer, John A; Hildebrandt, Friedhelm (2007). Mutation analysis of NPHP6/CEP290 in patients with Joubert syndrome and Senior-Løken syndrome. Journal of medical genetics, 44(10), pp. 657-63. London: BMJ Publishing Group 10.1136/jmg.2007.052027
