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Pontz, B.
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1

Osteogenesis imperfecta and hyperplastic callus formation: ..:

Stöss, H. ; Pontz, B. ; Vetter, U....
American Journal of Medical Genetics.  45 (1993)  2 - p. 260-260 , 1993
Link: https://doi.org/10.1002/..
 
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2

Pathologisch-anatomische Befunde am Callus bei Osteogenesis..:

, In: Aktuelle Aspekte der Osteologie,
Stöß, H. ; Pontz, B. ; Brenner, R.... - p. 264-270 , 1992
Link: https://doi.org/10.1007/..
 
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3

Osteogenesis imperfecta: A clinical study of the first ten ..:

Vetter, U. ; Pontz, B. ; Zauner, E...
Calcified Tissue International.  50 (1992)  1 - p. 36-41 , 1992
Link: https://doi.org/10.1007/..
 
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4

Wolcott-Rallison syndrome: Diabetes mellitus and spondyloep..:

Stöß, H. ; Pesch, H. -J. ; Pontz, B...
European Journal of Pediatrics.  138 (1982)  2 - p. 120-129 , 1982
Link: https://doi.org/10.1007/..
 
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5

Differentiation at the molecular level between various anti..:

Furthmayr, H. ; Pontz, B. ; Meigel, W...
Immunochemistry.  7 (1970)  10 - p. 859 , 1970
Link: https://doi.org/10.1016/..
 
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6

Aggressive Zytostatikatherapie osteogener Sarkome im Kindes..:

Pontz, B. F. ; Gutjahr, P.
DMW - Deutsche Medizinische Wochenschrift.  106 (2008)  7 - p. 200-207 , 2008
Link: https://doi.org/10.1055/..
 
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7

32-j�hriger Patient mit pathologischer Humerusfraktur, Sple..:

D�rr, E. M. ; Gei�, H. C. ; Pontz, B. F..
Der Internist.  45 (2004)  4 - p. 455-460 , 2004
Link: https://doi.org/10.1007/..
 
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8

Detection of neonatal argininosuccinate lyase deficiency by..:

Stadler, S. ; Gempel, K. ; Bieger, I....
Journal of Inherited Metabolic Disease.  24 (2001)  3 - p. 370-378 , 2001
Link: https://doi.org/10.1023/..
 
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9

Symptomatic ornithine carbamoyltransferase deficiency (poin..:

Staudt, M. ; Wermuth, B. ; Freisinger, P...
Journal of Inherited Metabolic Disease.  21 (1998)  1 - p. 71-72 , 1998
Link: https://doi.org/10.1023/..
 
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10

Familial insulin resistant diabetes associated with acantho..:

Boor, R. ; Herwig, J. ; Schrezenmeir, J...
American Journal of Medical Genetics.  45 (1993)  5 - p. 649-653 , 1993
Link: https://doi.org/10.1002/..
 
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11

Lymphadenopathy in connection with human herpes virus type ..:

Stettner-Gloning, R. ; J�ger, G. ; Gloning, H...
The Clinical Investigator.  70 (1992)  1 - p. 59-62 , 1992
Link: https://doi.org/10.1007/..
 
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12

Prenatal diagnosis of galactosialidosis:

Sewell, A. C. ; Pontz, B. F.
Prenatal Diagnosis.  8 (1988)  2 - p. 151-155 , 1988
Link: https://doi.org/10.1002/..
 
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13

Clinical heterogeneity in infantile galactosialidosis:

Sewell, A. C. ; Pontz, B. F. ; Weitzel, D..
European Journal of Pediatrics.  146 (1987)  5 - p. 528-531 , 1987
Link: https://doi.org/10.1007/..
 
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14

Biochemical, morphological and immunological findings in a ..:

Pontz, B. F. ; Zepp, F. ; St��, H.
European Journal of Pediatrics.  145 (1986)  5 - p. 428-434 , 1986
Link: https://doi.org/10.1007/..
 
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15

Heterogeneity of osteogenesis imperfecta. Biochemical and m..:

St��, H. ; Pontz, B. F. ; Pesch, H. -J..
European Journal of Pediatrics.  145 (1986)  1-2 - p. 34-39 , 1986
Link: https://doi.org/10.1007/..
 
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