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Prenatal Diagnosis
|
May 22, 2001
Current awareness in prenatal diagnosis
L C Horn, R Faber, A Meiner, et al.
Archives of Gynecology and Obstetrics
|
August 29, 2002
Malformations in newborn: results based on 30,940 infants and fetuses from the Mainz congenital birth defect monitoring system (1990-1998)
A Queisser-Luft, G Stolz, A Wiesel, et al.
European Journal of Pediatrics
|
June 1, 1983
Heterogeneity of metatropic dysplasia
M Beck, M Roubicek, J G Rogers, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1981
Aspartylglycosaminuria in an Italian family: clinical and biochemical characteristics
J Gehler, A C Sewell, C Becker, et al.
Helvetica Paediatrica Acta
|
January 1, 1981
Clinical and biochemical delineation of aspartyl-glycosaminuria as observed in two members of an Italian family
J Gehler, A C Sewell, C Becker, et al.
Prenatal Diagnosis
|
December 13, 2000
Greenberg dysplasia: first reported case with additional non-skeletal malformations and without consanguinity
L C Horn, R Faber, A Meiner, et al.
Birth Defects Original Article Series
|
January 1, 1975
Mannosidosis: clinical and biochemical findings
J Gehler, M Cantz, J F O'Brien, et al.
Calcified Tissue International
|
January 1, 1992
Osteogenesis imperfecta: a clinical study of the first ten years of life
U Vetter, B Pontz, E Zauner, et al.
American Journal of Medical Genetics. Part A
|
May 12, 2005
Autosomal dominant inheritance of spondyloenchondrodysplasia
R Bhargava, N J Leonard, A K J Chan, et al.
Medizinische Klinik (Munich, Germany : 1983)
|
March 1, 1995
[TNF-alpha level in the vitreous body. Increase in neovascular eye diseases and proliferative diabetic retinopathy]
J Spranger, R Meyer-Schwickerath, M Klein, et al.
Page
of 25
Search research articles
Search
Showing results (141-150 of 247) with videos related to
Sort By:
Page
of 25
Prenatal Diagnosis
|
May 22, 2001
Current awareness in prenatal diagnosis
L C Horn, R Faber, A Meiner, et al.
Archives of Gynecology and Obstetrics
|
August 29, 2002
Malformations in newborn: results based on 30,940 infants and fetuses from the Mainz congenital birth defect monitoring system (1990-1998)
A Queisser-Luft, G Stolz, A Wiesel, et al.
European Journal of Pediatrics
|
June 1, 1983
Heterogeneity of metatropic dysplasia
M Beck, M Roubicek, J G Rogers, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1981
Aspartylglycosaminuria in an Italian family: clinical and biochemical characteristics
J Gehler, A C Sewell, C Becker, et al.
Helvetica Paediatrica Acta
|
January 1, 1981
Clinical and biochemical delineation of aspartyl-glycosaminuria as observed in two members of an Italian family
J Gehler, A C Sewell, C Becker, et al.
Prenatal Diagnosis
|
December 13, 2000
Greenberg dysplasia: first reported case with additional non-skeletal malformations and without consanguinity
L C Horn, R Faber, A Meiner, et al.
Birth Defects Original Article Series
|
January 1, 1975
Mannosidosis: clinical and biochemical findings
J Gehler, M Cantz, J F O'Brien, et al.
Calcified Tissue International
|
January 1, 1992
Osteogenesis imperfecta: a clinical study of the first ten years of life
U Vetter, B Pontz, E Zauner, et al.
American Journal of Medical Genetics. Part A
|
May 12, 2005
Autosomal dominant inheritance of spondyloenchondrodysplasia
R Bhargava, N J Leonard, A K J Chan, et al.
Medizinische Klinik (Munich, Germany : 1983)
|
March 1, 1995
[TNF-alpha level in the vitreous body. Increase in neovascular eye diseases and proliferative diabetic retinopathy]
J Spranger, R Meyer-Schwickerath, M Klein, et al.
Page
of 25