J. Robert

发表

[Registries of malformations in the Rhône-Alps/Auvergne region. Value and limits of monitoring teratogenesis. 11 years' experience (1976-1986)].

C. Francannet, E. Robert, J. Robert, 1988, Journal de gynecologie, obstetrique et biologie de la reproduction.

Fraser syndrome with renal agenesis in two consanguineous Turkish families.

P. Lefrançois, C. Francannet, P. Dechelotte, 1990, American journal of medical genetics.

H. Plauchu, J. de Chadarévian, A. Bideau, 1989, American journal of medical genetics.

[PSYCHOPHARMACOLOGY AND TERATOGENESIS; SUMMARY OF A PRELIMINARY CLINICAL SURVEY].

J. Robert, M. Favre-Tissot, P. Broussolle, 1964, Annales Medico-Psychologiques.

[Genetic aspects of Rendu-Osler disease in Haut-Jura: convergence of methodological approaches of historic demography and medical genetics].

A. Jacquard, H. Plauchu, B. Desjardins, 1980, Journal de genetique humaine.

Genealogical study of oculopharyngeal muscular dystrophy in France

B. Eymard, M. Fardeau, F. Tomé, 1997, Neuromuscular Disorders.

Diffusion of a particular 4.1(−) hereditary elliptocytosis allele in the French northern Alps

J. Delaunay, F. Baklouti, L. Roda, 1993, Journal of Biosocial Science.

An abnormal concentration of cases of Rendu-Osler disease in the Valserine valley of the French Jura: a genealogical and demographic study.

E. Heyer, H. Plauchu, A. Bideau, 1992, Annals of human biology.

[Oculopharyngeal muscular dystrophy. A census of French families and genealogic study].

M. Fardeau, F. Tomé, F. Samson, 1990, Revue neurologique.

[Meckel's syndrome].

F. Freycon, B. Lauras, J. Fraisse, 1976, Pediatrie.

Molecular analysis of hereditary elliptocytosis with reduced protein 4.1 in the French Northern Alps.

E. Benz, N. Alloisio, S. Chabanis, 1991, Blood.

Rectocolic familial polyposis; a study of 32 cases

H. Plauchu, P. Bérard, J. Robert, 1981, World Journal of Surgery.

Confirmation of the assignment of the human SODS gene to chromosome 21q22.

P. Sinet, F. Freycon, T. Philip, 1978, Cytogenetics and cell genetics.

Genetic Counseling in Chromosomal Aberrations in Neurology and Ophthalmology

C. Laurent, J. Pernod, J. Robert, 1974 .

[Chromosomal anomalies in Fanconi's anemia (6 personal cases)].

F. Freycon, D. Germain, J. Viala, 1968, Pediatrie.

[Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10), rec(10), in her son (author's transl)].

B. Dutrillaux, J. Lejeune, C. Laurent, 1973, Cytogenetics and cell genetics.

[Clinical and cytogenetic observations on 2 mosaic C trisomic adults. Individualization of the supernumerary chromosome with the modern denaturation technic: 47, XY, ?8 +].

B. Dutrillaux, C. Laurent, J. Robert, 1971, Lyon medical.

Observations cliniques et cytogénétiques de deux adultes trisomiques C en mosaïque. Individualisation du chromosome surnuméraire par la technique moderne de dénaturation: 47, XY, ?8.

B. Dutrillaux, C. Laurent, J. Robert, 1971 .

[Essential acro-osteolysis of carpal and tarsal onset with nephropathy].

P. Zech, D. Fries, J. Traeger, 1971, Archives francaises de pediatrie.

[Thanatophoric dwarfism].

M. Lamy, P. Maroteaux, J. Robert, 1967, La Presse medicale.

Epidemiological investigation of Rendu-Osler disease in France: its geographical distribution and prevalence.

H. Plauchu, A. Bideau, G. Brunet, 1989, Population. English selection.

[International Clearinghouse for Birth Defects Monitoring Systems (ICBDMS). An example of effective international cooperation].

C. Francannet, E. Robert, J. Robert, 1986, Archives francaises de pediatrie.

Evaluation of drug therapy and teratogenic risk in a Rhône-Alpes district population of pregnant epileptic women.

F. Mauguière, E. Robert, J. Robert, 1986, European neurology.

SYSTEMATIC NEONATAL SCREENING FOR DUCHENNE MUSCULAR DYSTROPHY

C. Dorche, C. Collombel, J. Cotte, 1978, The Lancet.

DUCHENNE MUSCULAR DYSTROPHY: NEONATAL SCREENING AND PRENATAL DIAGNOSIS

H. Plauchu, M. Cordier, C. Dorche, 1989, The Lancet.

Structured Lower Rank ApproximationMoody

T. Chu, E. Robert, Funderlicy, 1998 .