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P Dodinval

Showing results (41-50 of 54) with videos related to

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American Journal of Medical Genetics|September 1, 1992
Glaucoma-lens ectopia-microspherophakia-stiffness-shortness (GEMSS) syndrome: a dominant disease with manifestations of Weill-Marchesani syndromesA Verloes, J P Hermia, A Galand, et al.
Clinical Genetics|March 1, 1989
3C syndrome: third occurrence of cranio-cerebello-cardiac dysplasia (Ritscher-Schinzel syndrome)A Verloes, M F Dresse, M Jovanovic, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1991
A hydropic fetus with translucent ribs, arthrogryposis multiplex congenita and congenital myopathy: etiological heterogeneity of A.M.C., Toriello-Bauserman type?A Verloes, P Dodinval, M C Retz, et al.
Annales De Genetique|January 1, 1989
Roberts-SC phocomelia syndrome with exencephalyA Verloes, C Herens, L Van Maldergem, et al.
Prenatal Diagnosis|February 1, 1991
Prenatal diagnosis of cystic hygroma and chorioangioma in the Wolf-Hirschhorn syndromeA Verloes, J P Schaaps, C Herens, et al.
Revue Medicale De Liege|September 1, 1982
[Alpha 1-antitrypsin deficiency: evaluation and perspectives. Apropos of 1000 instances of assay and genetic typing]C Rorive, R Schoos, J Dodinval-Versie, et al.
Acta Neuropathologica|January 1, 1981
Fetal Krabbe leukodystrophy. A morphologic study of two casesJ J Martin, J G Leroy, C Ceuterick, et al.
Clinical Genetics|May 1, 1988
Partial trisomy 20q due to paternal t(8;20) translocation. Case report and review of the literatureG Pierquin, C Herens, P Dodinval, et al.
Dermatologica|January 1, 1990
Poikiloderma, alopecia, retrognathism and cleft palate: the PARC syndrome. Is this an undescribed dominantly inherited syndrome?A Verloes, M Soyeur-Broux, J Arrese-Estrada, et al.
American Journal of Human Genetics|July 1, 1973
Genetic structure of SwitzerlandN E Morton, D Klein, I E Hussels, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics|September 1, 1992
Glaucoma-lens ectopia-microspherophakia-stiffness-shortness (GEMSS) syndrome: a dominant disease with manifestations of Weill-Marchesani syndromesA Verloes, J P Hermia, A Galand, et al.
Clinical Genetics|March 1, 1989
3C syndrome: third occurrence of cranio-cerebello-cardiac dysplasia (Ritscher-Schinzel syndrome)A Verloes, M F Dresse, M Jovanovic, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1991
A hydropic fetus with translucent ribs, arthrogryposis multiplex congenita and congenital myopathy: etiological heterogeneity of A.M.C., Toriello-Bauserman type?A Verloes, P Dodinval, M C Retz, et al.
Annales De Genetique|January 1, 1989
Roberts-SC phocomelia syndrome with exencephalyA Verloes, C Herens, L Van Maldergem, et al.
Prenatal Diagnosis|February 1, 1991
Prenatal diagnosis of cystic hygroma and chorioangioma in the Wolf-Hirschhorn syndromeA Verloes, J P Schaaps, C Herens, et al.
Revue Medicale De Liege|September 1, 1982
[Alpha 1-antitrypsin deficiency: evaluation and perspectives. Apropos of 1000 instances of assay and genetic typing]C Rorive, R Schoos, J Dodinval-Versie, et al.
Acta Neuropathologica|January 1, 1981
Fetal Krabbe leukodystrophy. A morphologic study of two casesJ J Martin, J G Leroy, C Ceuterick, et al.
Clinical Genetics|May 1, 1988
Partial trisomy 20q due to paternal t(8;20) translocation. Case report and review of the literatureG Pierquin, C Herens, P Dodinval, et al.
Dermatologica|January 1, 1990
Poikiloderma, alopecia, retrognathism and cleft palate: the PARC syndrome. Is this an undescribed dominantly inherited syndrome?A Verloes, M Soyeur-Broux, J Arrese-Estrada, et al.
American Journal of Human Genetics|July 1, 1973
Genetic structure of SwitzerlandN E Morton, D Klein, I E Hussels, et al.
Pageof 6