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E Passarge

Showing results (121-130 of 151) with videos related to

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Casopis Lekaru Ceskych|August 2, 1985
[The 47,XXX syndrome in a family with the fragile X chromosome syndrome]E Seemanová, A Schmidt, I Subrt, et al.
Andrologie|January 1, 1973
[Werner's syndrome. A hereditable disorder of multiple organsystems (author's transl)]D Kulenkamp, D Scholz-Jordan, E Passarge, et al.
Birth Defects Original Article Series|January 1, 1975
Two male sibs with a previously unrecognized syndrome: facial dysmorphia, hyperextensibility of joints, clinodactyly, growth retardation and mental retardationG Morillo-Cucci, E Passarge, J L Simpson, et al.
Human Genetics|July 1, 1989
Maternal origin of a de novo chromosome 8 deletion in a patient with Langer-Giedion syndromeH J Lüdecke, R Burdiek, G Senger, et al.
Immunology Letters|November 1, 1990
Further characterization of the EAI factor induced by alloimmunization for treatment of recurrent abortionR Blasczyk, U Kuhn, W Luboldt, et al.
Birth Defects Original Article Series|January 1, 1975
A patient with the Larsen syndromeJ L Simpson, E Passarge, P Hathaway, et al.
American Journal of Medical Genetics|February 15, 1993
New autosomal recessive lethal disorder with polycystic kidneys type Potter I, characteristic face, microcephaly, brachymelia, and congenital heart defectsG Gillessen-Kaesbach, P Meinecke, C Garrett, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 30, 1973
Rapid diagnosis of maple syrup urine disease (branched chain ketoaciduria) by micro-enzyme assay in leukocytes and fibroblastsU Wendel, W Wöhler, H W Goedde, et al.
Casopis Lekaru Ceskych|February 18, 1983
[Macro-orchism. A significant symptom in the detection of the fragile X chromosome syndrome]E Seemanová, A Schmidt, K Popelová, et al.
Deutsche Medizinische Wochenschrift (1946)|June 7, 1974
[Familial Alport's syndrome with anterior lenticonus (author's transl)]K Dahm, H R Koch, M Siedek, et al.
Pageof 16

Showing results (121-130 of 151) with videos related to

Sort By:
Pageof 16
Casopis Lekaru Ceskych|August 2, 1985
[The 47,XXX syndrome in a family with the fragile X chromosome syndrome]E Seemanová, A Schmidt, I Subrt, et al.
Andrologie|January 1, 1973
[Werner's syndrome. A hereditable disorder of multiple organsystems (author's transl)]D Kulenkamp, D Scholz-Jordan, E Passarge, et al.
Birth Defects Original Article Series|January 1, 1975
Two male sibs with a previously unrecognized syndrome: facial dysmorphia, hyperextensibility of joints, clinodactyly, growth retardation and mental retardationG Morillo-Cucci, E Passarge, J L Simpson, et al.
Human Genetics|July 1, 1989
Maternal origin of a de novo chromosome 8 deletion in a patient with Langer-Giedion syndromeH J Lüdecke, R Burdiek, G Senger, et al.
Immunology Letters|November 1, 1990
Further characterization of the EAI factor induced by alloimmunization for treatment of recurrent abortionR Blasczyk, U Kuhn, W Luboldt, et al.
Birth Defects Original Article Series|January 1, 1975
A patient with the Larsen syndromeJ L Simpson, E Passarge, P Hathaway, et al.
American Journal of Medical Genetics|February 15, 1993
New autosomal recessive lethal disorder with polycystic kidneys type Potter I, characteristic face, microcephaly, brachymelia, and congenital heart defectsG Gillessen-Kaesbach, P Meinecke, C Garrett, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 30, 1973
Rapid diagnosis of maple syrup urine disease (branched chain ketoaciduria) by micro-enzyme assay in leukocytes and fibroblastsU Wendel, W Wöhler, H W Goedde, et al.
Casopis Lekaru Ceskych|February 18, 1983
[Macro-orchism. A significant symptom in the detection of the fragile X chromosome syndrome]E Seemanová, A Schmidt, K Popelová, et al.
Deutsche Medizinische Wochenschrift (1946)|June 7, 1974
[Familial Alport's syndrome with anterior lenticonus (author's transl)]K Dahm, H R Koch, M Siedek, et al.
Pageof 16