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Schweizerische Rundschau Fur Medizin Praxis = Revue Suisse De Medecine Praxis
|
July 5, 1977
[Current genetic problems of hemophilia and detection of carriers (author's transl)]
J P Marcoz
Journal De Genetique Humaine
|
September 1, 1978
[Screening for heterozygotes in a large family suffering from Steinert's disease with varying clinical manifestations (author's transl)]
J P Marcoz
Revue Medicale De La Suisse Romande
|
August 1, 1978
[Myotonic dystrophy with a variable symptomatology and favorable clinical prognosis in a large family]
J P Marcoz, D Klein
Archiv Fur Genetik
|
January 1, 1978
[Study of two brothers with XYY karyotype including one with mosaicism]
J P Marcoz, D Bourquin, L Crippa
Journal De Genetique Humaine
|
June 1, 1978
[Do all cases of trisomy 18 with long survival (beyond 10 years) show mosaicism in fibroblasts? (author's transl)]
L Crippa, J P Marcoz, D Klein, et al.
Revue Medicale De La Suisse Romande
|
May 1, 1980
[Neonatal case finding in hip abnormalities]
J P Marcoz, A Spahr, G Délèze, et al.
Neuropediatrics
|
April 1, 1993
Speech and oromotor deficits of epileptic origin in benign partial epilepsy of childhood with rolandic spikes (BPERS). Relationship to the acquired aphasia-epilepsy syndrome
T W Deonna, E Roulet, D Fontan, et al.
Schweizerische Rundschau Fur Medizin Praxis = Revue Suisse De Medecine Praxis
|
July 27, 1982
[Final result of a clinical, genetic and cytogenetic investigation of 182 mentally retarded patients of a medico-educative institution]
D Klein, J P Marcoz, R L Mounoud, et al.
Schweizerische Rundschau Fur Medizin Praxis = Revue Suisse De Medecine Praxis
|
July 13, 1982
[Final results of a clinical, genetic and cytogenetic study of 182 oligophrenic patients in a medico-educational institution. 1]
D Klein, J P Marcoz, R L Mounoud, et al.
Klinische Monatsblatter Fur Augenheilkunde
|
May 1, 1997
[Ocular phenotype in a child with chondrodysplasia punctata, rhizomelic form]
E Sanchez, F Munier, B Evéquoz, et al.
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of 2
Search research articles
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Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Schweizerische Rundschau Fur Medizin Praxis = Revue Suisse De Medecine Praxis
|
July 5, 1977
[Current genetic problems of hemophilia and detection of carriers (author's transl)]
J P Marcoz
Journal De Genetique Humaine
|
September 1, 1978
[Screening for heterozygotes in a large family suffering from Steinert's disease with varying clinical manifestations (author's transl)]
J P Marcoz
Revue Medicale De La Suisse Romande
|
August 1, 1978
[Myotonic dystrophy with a variable symptomatology and favorable clinical prognosis in a large family]
J P Marcoz, D Klein
Archiv Fur Genetik
|
January 1, 1978
[Study of two brothers with XYY karyotype including one with mosaicism]
J P Marcoz, D Bourquin, L Crippa
Journal De Genetique Humaine
|
June 1, 1978
[Do all cases of trisomy 18 with long survival (beyond 10 years) show mosaicism in fibroblasts? (author's transl)]
L Crippa, J P Marcoz, D Klein, et al.
Revue Medicale De La Suisse Romande
|
May 1, 1980
[Neonatal case finding in hip abnormalities]
J P Marcoz, A Spahr, G Délèze, et al.
Neuropediatrics
|
April 1, 1993
Speech and oromotor deficits of epileptic origin in benign partial epilepsy of childhood with rolandic spikes (BPERS). Relationship to the acquired aphasia-epilepsy syndrome
T W Deonna, E Roulet, D Fontan, et al.
Schweizerische Rundschau Fur Medizin Praxis = Revue Suisse De Medecine Praxis
|
July 27, 1982
[Final result of a clinical, genetic and cytogenetic investigation of 182 mentally retarded patients of a medico-educative institution]
D Klein, J P Marcoz, R L Mounoud, et al.
Schweizerische Rundschau Fur Medizin Praxis = Revue Suisse De Medecine Praxis
|
July 13, 1982
[Final results of a clinical, genetic and cytogenetic study of 182 oligophrenic patients in a medico-educational institution. 1]
D Klein, J P Marcoz, R L Mounoud, et al.
Klinische Monatsblatter Fur Augenheilkunde
|
May 1, 1997
[Ocular phenotype in a child with chondrodysplasia punctata, rhizomelic form]
E Sanchez, F Munier, B Evéquoz, et al.
Page
of 2