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American Journal of Medical Genetics
|
July 3, 1995
Two sisters with Escobar syndrome
S Spranger, M Spranger, H M Meinck, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
September 1, 1989
Acrorenal syndrome in an adult--presentation with proteinuria, hypertension, and glomerular lesions
M Zeier, G Tariverdian, R Waldherr, et al.
American Journal of Medical Genetics
|
May 3, 1996
Bilateral radial deficiency with lower limb involvement
S Spranger, M Weber, J Tröger, et al.
American Journal of Medical Genetics
|
March 9, 1999
Rare dental abnormalities seen in oculo-facio-cardio-dental (OFCD) syndrome: three new cases and review of nine patients
B R Schulze, D Horn, A Kobelt, et al.
Clinical Genetics
|
May 1, 1997
Molecular studies of an X;Y translocation chromosome in a woman with deletion of the pseudoautosomal region but normal height
S Spranger, S Kirsch, A Mertz, et al.
American Journal of Medical Genetics
|
December 8, 1998
Short-rib-polydactyly syndrome type Verma-Naumoff-Le Marec in a fetus with histological hallmarks of type Saldino-Noonan but lacking internal organ abnormalities
S Hentze, C Sergi, J Troeger, et al.
Zeitschrift Fur Geburtshilfe Und Perinatologie
|
September 1, 1988
[Transabdominal chorionic villi aspiration in the 1st and 2d trimester in 120 cases with reference to placental location]
J Klapp, G Tariverdian, J Greiner, et al.
European Journal of Pediatrics
|
September 1, 1996
Case report. Microcephalic osteodysplastic primordial dwarfism type II: a child with unusual symptoms and clinical course
S Spranger, G Tariverdian, F K Albert, et al.
Geburtshilfe Und Frauenheilkunde
|
November 1, 1987
[Transabdominal chorionic biopsy: indications and timing of the procedure]
J Klapp, G Tariverdian, H D Hager, et al.
American Journal of Medical Genetics
|
April 6, 2000
A case of Perlman syndrome: fetal gigantism, renal dysplasia, and severe neurological deficits
K Schilke, F Schaefer, R Waldherr, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 30) with videos related to
Sort By:
Page
of 3
American Journal of Medical Genetics
|
July 3, 1995
Two sisters with Escobar syndrome
S Spranger, M Spranger, H M Meinck, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
September 1, 1989
Acrorenal syndrome in an adult--presentation with proteinuria, hypertension, and glomerular lesions
M Zeier, G Tariverdian, R Waldherr, et al.
American Journal of Medical Genetics
|
May 3, 1996
Bilateral radial deficiency with lower limb involvement
S Spranger, M Weber, J Tröger, et al.
American Journal of Medical Genetics
|
March 9, 1999
Rare dental abnormalities seen in oculo-facio-cardio-dental (OFCD) syndrome: three new cases and review of nine patients
B R Schulze, D Horn, A Kobelt, et al.
Clinical Genetics
|
May 1, 1997
Molecular studies of an X;Y translocation chromosome in a woman with deletion of the pseudoautosomal region but normal height
S Spranger, S Kirsch, A Mertz, et al.
American Journal of Medical Genetics
|
December 8, 1998
Short-rib-polydactyly syndrome type Verma-Naumoff-Le Marec in a fetus with histological hallmarks of type Saldino-Noonan but lacking internal organ abnormalities
S Hentze, C Sergi, J Troeger, et al.
Zeitschrift Fur Geburtshilfe Und Perinatologie
|
September 1, 1988
[Transabdominal chorionic villi aspiration in the 1st and 2d trimester in 120 cases with reference to placental location]
J Klapp, G Tariverdian, J Greiner, et al.
European Journal of Pediatrics
|
September 1, 1996
Case report. Microcephalic osteodysplastic primordial dwarfism type II: a child with unusual symptoms and clinical course
S Spranger, G Tariverdian, F K Albert, et al.
Geburtshilfe Und Frauenheilkunde
|
November 1, 1987
[Transabdominal chorionic biopsy: indications and timing of the procedure]
J Klapp, G Tariverdian, H D Hager, et al.
American Journal of Medical Genetics
|
April 6, 2000
A case of Perlman syndrome: fetal gigantism, renal dysplasia, and severe neurological deficits
K Schilke, F Schaefer, R Waldherr, et al.
Page
of 3