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Entries: 1-4  
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Hypergonadotropic hypogonadism in a patient with inv ins (2;4)
Authors: Tzschach, A.; Ramel, C.; Kron, A.; Seipel, B.; Wüster, C.; Cordes, U.; Liehr, T.; Hoeltzenbein, M.; Menzel, C.; Ropers, H.-H.; Ullmann, R.; Kalscheuer, V.; Decker, J.; Steinberger, D.
Date of Publication (YYYY-MM-DD): 2009-06
Title of Journal: International Journal of Andrology
Volume: 32
Issue / Number: 3
Start Page: 226
End Page: 230
Document Type: Article
ID: 473660.0
Schnyder's crystalline corneal dystrophy. Further narrowing of the linkage interval at chromosome 1p34.1-p36?
Authors: Riebeling, P.; Polz, S.; Tost, F.; Weiss, J. S.; Kuivaniemi, H.; Hoeltzenbein, M.
Date of Publication (YYYY-MM-DD): 2003-11
Title of Journal: Ophthalmologe
Volume: 100
Issue / Number: 11
Start Page: 979
End Page: 983
Document Type: Article
ID: 127787.0
Lhermitte-Duclos disease in 3 children: A clinical long-term observation
Authors: Mori, A. C.; Hoeltzenbein, M.; Poetsch, M.; Schneider, J. F.; Brandner, S.; Boltshauser, E.
Date of Publication (YYYY-MM-DD): 2003-02
Title of Journal: Neuropediatrics
Volume: 34
Issue / Number: 1
Start Page: 30
End Page: 35
Document Type: Article
ID: 127774.0
Childhood onset mitochondrial myopathy and lactic
acidosis caused by a stop mutation in the mitochondrial
cytochrome c oxidase III gene
Authors: Horváth, R.; Scharfe, C.; Hoeltzenbein, M.; Do, B. H.; Schröder, C.; Warzok, R.; Vogelgesang, S.; Lochmüller, H.; Müller-Höcker, J.; Gerbitz, K. D.; Oefner, P. J.; Jaksch, M.
Date of Publication (YYYY-MM-DD): 2002-11
Title of Journal: Journal of Medical Genetics
Volume: 39
Issue / Number: 11
Start Page: 812
End Page: 816
Document Type: Article
ID: 24161.0
Entries: 1-4  
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