K R Held - JoVE Visualize

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Andrologia|May 1, 1980

[XX-male syndrome from the andrologic viewpoint]H Pusch, K R Held, C Schirren, et al.

Cytotechnology|January 1, 1990

Clonal derivatives of a human B-lymphoblastoid cell line producing prolactin--a cytogenetic characterizationA Bonhoff, B Gellersen, K R Held, et al.

Teratology|October 1, 1981

Congenital malformation syndromes and elevation of amniotic fluid alpha-fetoproteinU Burck, K R Held, H J Kitschke, et al.

Clinical Genetics|March 1, 1977

Genetic heterogeneity of hypoxanthine-phosphoribosyl transferase in human fibroblasts of 3 familiesI Willers, K R Held, S Singh, et al.

Wiener Klinische Wochenschrift|May 15, 1981

[Investigation of a variant form of hypoxanthine-phosphoribosyl transferase in a family (author's transl)]I Willers, K R Held, S Singh, et al.

Monatsschrift Fur Kinderheilkunde|February 1, 1976

[Intermittent branched--chain ketoacidurie in ketotic hypoglycemia: investigations to localize the biochemical defect (author's transl)]K R Held, H J Sternowsky, S Singh, et al.

European Journal of Pediatrics|January 1, 1985

A case of lipogranulomatosis Farber: some clinical and ultrastructural aspectsU Burck, H W Moser, H H Goebel, et al.

Geburtshilfe Und Frauenheilkunde|December 1, 1990

[Early amniocentesis for cytogenetic diagnosis]C Lindner, B Hüneke, D Masson, et al.

Annals of Hematology|January 1, 1993

Atypical chronic myelogenous leukemia in a patient with trisomy 8 mosaicism syndromeP Kapaun, H Kabisch, K R Held, et al.

Neuropadiatrie|May 1, 1980

Ultrastructural pathology of skin biopsy and fibroblast enzyme studies in a case of GM2-gangliosidosis with deficient hexosaminidase A and thermolabile hexosaminidase BU Burck, K Harzer, H H Goebel, et al.

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Showing results (21-30 of 36) with videos related to

Sort By:

Pageof 4

Andrologia|May 1, 1980

[XX-male syndrome from the andrologic viewpoint]H Pusch, K R Held, C Schirren, et al.

Cytotechnology|January 1, 1990

Clonal derivatives of a human B-lymphoblastoid cell line producing prolactin--a cytogenetic characterizationA Bonhoff, B Gellersen, K R Held, et al.

Teratology|October 1, 1981

Congenital malformation syndromes and elevation of amniotic fluid alpha-fetoproteinU Burck, K R Held, H J Kitschke, et al.

Clinical Genetics|March 1, 1977

Genetic heterogeneity of hypoxanthine-phosphoribosyl transferase in human fibroblasts of 3 familiesI Willers, K R Held, S Singh, et al.

Wiener Klinische Wochenschrift|May 15, 1981

[Investigation of a variant form of hypoxanthine-phosphoribosyl transferase in a family (author's transl)]I Willers, K R Held, S Singh, et al.

Monatsschrift Fur Kinderheilkunde|February 1, 1976

[Intermittent branched--chain ketoacidurie in ketotic hypoglycemia: investigations to localize the biochemical defect (author's transl)]K R Held, H J Sternowsky, S Singh, et al.

European Journal of Pediatrics|January 1, 1985

A case of lipogranulomatosis Farber: some clinical and ultrastructural aspectsU Burck, H W Moser, H H Goebel, et al.

Geburtshilfe Und Frauenheilkunde|December 1, 1990

[Early amniocentesis for cytogenetic diagnosis]C Lindner, B Hüneke, D Masson, et al.

Annals of Hematology|January 1, 1993

Atypical chronic myelogenous leukemia in a patient with trisomy 8 mosaicism syndromeP Kapaun, H Kabisch, K R Held, et al.

Neuropadiatrie|May 1, 1980

Ultrastructural pathology of skin biopsy and fibroblast enzyme studies in a case of GM2-gangliosidosis with deficient hexosaminidase A and thermolabile hexosaminidase BU Burck, K Harzer, H H Goebel, et al.

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