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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 retardation
G 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 syndrome
H 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 abortion
R Blasczyk, U Kuhn, W Luboldt, et al.
Birth Defects Original Article Series
|
January 1, 1975
A patient with the Larsen syndrome
J 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 defects
G 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 fibroblasts
U 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.
Page
of 16
Search research articles
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Showing results (121-130 of 151) with videos related to
Sort By:
Page
of 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 retardation
G 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 syndrome
H 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 abortion
R Blasczyk, U Kuhn, W Luboldt, et al.
Birth Defects Original Article Series
|
January 1, 1975
A patient with the Larsen syndrome
J 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 defects
G 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 fibroblasts
U 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.
Page
of 16