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Kinderarztliche Praxis
|
May 1, 1989
[Familial Noonan syndrome]
G Krüger, K Schumacher, M Mix, et al.
Human Genetics
|
December 1, 1988
Increased methotrexate-induced chromosome breakage in patients with free trisomy 21 and their parents
L Pelz, J Götz, G Krüger, et al.
American Journal of Medical Genetics
|
June 1, 1993
Cytomegalic type of congenital adrenal hypoplasia due to autosomal recessive inheritance
G Krüger, M Mix, L Pelz, et al.
European Journal of Pediatrics
|
October 1, 1991
Mitral valve and tricuspidal valve prolapse in Melnick-Needles syndrome
G Krüger, K Schumacher, F Erfurt, et al.
Kinderarztliche Praxis
|
May 1, 1989
[Cytogenetic detection of Prader-Willi syndrome in infancy]
J Götz, G Krüger, B C Westphal, et al.
Acta Universitatis Palackianae Olomucensis Facultatis Medicae
|
January 1, 1981
Responsiveness of the pituitary to stimulation with arginine, GRH and TRH in patients with Turner's syndrome (karyotype 45, XO)
S Kunkel, K Rudolf, H Kyank, et al.
Acta Universitatis Palackianae Olomucensis Facultatis Medicae
|
January 1, 1981
Responsiveness of the pituitary to stimulation with arginine, GRH and TRH in patients with Turner' syndrome (karyotype 45, XO)
S Kunkel, K Rudolf, H Kyank, et al.
Kinderarztliche Praxis
|
February 1, 1971
[Orofaciodigital syndrome]
M Hille, L Pelz, A Andrä, et al.
Zeitschrift Fur Arztliche Fortbildung
|
June 15, 1982
[Retinopathy of the premature: possibility and limitations of prevention, therapy and metaphylaxis]
M Uhlemann, C Plath, J Eichler, et al.
Zentralblatt Fur Gynakologie
|
August 10, 1973
[Pregnancies following methotrexate treatmnet. Chromosome analysis in mother and child]
W D Junge, H Kyank, L Pelz, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 68) with videos related to
Sort By:
Page
of 7
Kinderarztliche Praxis
|
May 1, 1989
[Familial Noonan syndrome]
G Krüger, K Schumacher, M Mix, et al.
Human Genetics
|
December 1, 1988
Increased methotrexate-induced chromosome breakage in patients with free trisomy 21 and their parents
L Pelz, J Götz, G Krüger, et al.
American Journal of Medical Genetics
|
June 1, 1993
Cytomegalic type of congenital adrenal hypoplasia due to autosomal recessive inheritance
G Krüger, M Mix, L Pelz, et al.
European Journal of Pediatrics
|
October 1, 1991
Mitral valve and tricuspidal valve prolapse in Melnick-Needles syndrome
G Krüger, K Schumacher, F Erfurt, et al.
Kinderarztliche Praxis
|
May 1, 1989
[Cytogenetic detection of Prader-Willi syndrome in infancy]
J Götz, G Krüger, B C Westphal, et al.
Acta Universitatis Palackianae Olomucensis Facultatis Medicae
|
January 1, 1981
Responsiveness of the pituitary to stimulation with arginine, GRH and TRH in patients with Turner's syndrome (karyotype 45, XO)
S Kunkel, K Rudolf, H Kyank, et al.
Acta Universitatis Palackianae Olomucensis Facultatis Medicae
|
January 1, 1981
Responsiveness of the pituitary to stimulation with arginine, GRH and TRH in patients with Turner' syndrome (karyotype 45, XO)
S Kunkel, K Rudolf, H Kyank, et al.
Kinderarztliche Praxis
|
February 1, 1971
[Orofaciodigital syndrome]
M Hille, L Pelz, A Andrä, et al.
Zeitschrift Fur Arztliche Fortbildung
|
June 15, 1982
[Retinopathy of the premature: possibility and limitations of prevention, therapy and metaphylaxis]
M Uhlemann, C Plath, J Eichler, et al.
Zentralblatt Fur Gynakologie
|
August 10, 1973
[Pregnancies following methotrexate treatmnet. Chromosome analysis in mother and child]
W D Junge, H Kyank, L Pelz, et al.
Page
of 7