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C Piussan

Showing results (11-20 of 112) with videos related to

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Bulletin Des Societes D'Ophtalmologie De France|October 1, 1987
[Incontinentia pigmenti. Apropos of a case]P Turut, P Dumont, C Piussan, et al.
Annales De Genetique|January 1, 1980
[Partial trisomy (10pter leads to 10q21) and partial monosomy (21pter leads to 21q21) due to a reciprocal balanced familial translocation (10;21)(q21;q21) (author's transl)]E Obry, C Piussan, B Risbourg, et al.
American Journal of Medical Genetics|June 1, 1985
Dermatoglyphics in Börjeson-Forssman-Lehmann syndromeD B Flannery, C Piussan, L E Wright
Journal De Genetique Humaine|January 1, 1985
[Cerebral and ocular abnormalities with anterior pituitary insufficiency of familial nature]J Weill, B Boudailliez, C Piussan, et al.
Archives Francaises De Pediatrie|November 1, 1990
[Waardenburg's syndrome and severe cyanotic cardiopathy]M Mathieu, E Bourges, F Caron, et al.
Archives Francaises De Pediatrie|June 1, 1975
[Bone dysplasia with dwarfism and diffuse skeletal alterations]C Piussan, P Maroteaux, I Castroviejo, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
A familial syndrome with micrognathia, cleft palate, short neck and stature, vertebral anomalies and mental retardationM Mathieu, A De Broca, H Bony, et al.
Pediatrie|April 1, 1975
[Proceedings: Transitory neonatal hyperthyroidism]B Risbourg, C Piussan, J C Boitieux, et al.
American Journal of Medical Genetics|August 9, 1996
Fragile X mutation and FG syndrome-like phenotypeC Piussan, M Mathieu, P Berquin, et al.
Pediatrie|June 1, 1970
[A case of thrombosis of the Sylvian artery revealing acute tuberculosis]C Piussan, O Fovet-Poingt, J L Christiaens, et al.
Pageof 12

Showing results (11-20 of 112) with videos related to

Sort By:
Pageof 12
Bulletin Des Societes D'Ophtalmologie De France|October 1, 1987
[Incontinentia pigmenti. Apropos of a case]P Turut, P Dumont, C Piussan, et al.
Annales De Genetique|January 1, 1980
[Partial trisomy (10pter leads to 10q21) and partial monosomy (21pter leads to 21q21) due to a reciprocal balanced familial translocation (10;21)(q21;q21) (author's transl)]E Obry, C Piussan, B Risbourg, et al.
American Journal of Medical Genetics|June 1, 1985
Dermatoglyphics in Börjeson-Forssman-Lehmann syndromeD B Flannery, C Piussan, L E Wright
Journal De Genetique Humaine|January 1, 1985
[Cerebral and ocular abnormalities with anterior pituitary insufficiency of familial nature]J Weill, B Boudailliez, C Piussan, et al.
Archives Francaises De Pediatrie|November 1, 1990
[Waardenburg's syndrome and severe cyanotic cardiopathy]M Mathieu, E Bourges, F Caron, et al.
Archives Francaises De Pediatrie|June 1, 1975
[Bone dysplasia with dwarfism and diffuse skeletal alterations]C Piussan, P Maroteaux, I Castroviejo, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
A familial syndrome with micrognathia, cleft palate, short neck and stature, vertebral anomalies and mental retardationM Mathieu, A De Broca, H Bony, et al.
Pediatrie|April 1, 1975
[Proceedings: Transitory neonatal hyperthyroidism]B Risbourg, C Piussan, J C Boitieux, et al.
American Journal of Medical Genetics|August 9, 1996
Fragile X mutation and FG syndrome-like phenotypeC Piussan, M Mathieu, P Berquin, et al.
Pediatrie|June 1, 1970
[A case of thrombosis of the Sylvian artery revealing acute tuberculosis]C Piussan, O Fovet-Poingt, J L Christiaens, et al.
Pageof 12