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Y Gillerot

Showing results (11-20 of 87) with videos related to

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Annales De Pediatrie|November 1, 1979
[Persistent interstitial pulmonary emphysema (author's transl)]A Bachy, P Gerard, Y Gillerot
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1984
[Pulmonary hypoplasia. Apropos of a case in twins]M Maréchal, Y Gillerot, R Chef
Journal De Genetique Humaine|June 1, 1982
[Meiotic chromosomes and masculine infertility: evaluation of results]L Koulischer, R Schoysman, Y Gillerot
Journal De Genetique Humaine|June 1, 1982
[Neonatal autopsy and genetic counseling. 350 cases]Y Gillerot, L Koulischer, J Hustin
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 12, 2004
[Childhood hypophosphatasia: a case report due to a novel mutation]C Draguet, Y Gillerot, E Mornet
Journal De Genetique Humaine|January 1, 1988
[Chromosome translocations: study of 232 cases originating from 144 families]Y Gillerot, L Koulischer, E Jauniaux
European Journal of Pediatrics|December 1, 1983
Lethal perinatal type II osteogenesis imperfecta in a family with a dominantly inherited type IY Gillerot, J M Druart, L Koulischer
Clinical Genetics|January 1, 1989
Neural tube defects and omphalocele in trisomy 18L van Maldergem, Y Gillerot, L Koulischer
Prenatal Diagnosis|August 1, 1992
Morphological features of a case of retinoic acid embryopathyL Van Maldergem, E Jauniaux, Y Gillerot
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1991
[Amniocentesis and trophoblastic biopsy. Comparison of results]C Gérard, Y Gillerot, L Koulischer, et al.
Pageof 9

Showing results (11-20 of 87) with videos related to

Sort By:
Pageof 9
Annales De Pediatrie|November 1, 1979
[Persistent interstitial pulmonary emphysema (author's transl)]A Bachy, P Gerard, Y Gillerot
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1984
[Pulmonary hypoplasia. Apropos of a case in twins]M Maréchal, Y Gillerot, R Chef
Journal De Genetique Humaine|June 1, 1982
[Meiotic chromosomes and masculine infertility: evaluation of results]L Koulischer, R Schoysman, Y Gillerot
Journal De Genetique Humaine|June 1, 1982
[Neonatal autopsy and genetic counseling. 350 cases]Y Gillerot, L Koulischer, J Hustin
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 12, 2004
[Childhood hypophosphatasia: a case report due to a novel mutation]C Draguet, Y Gillerot, E Mornet
Journal De Genetique Humaine|January 1, 1988
[Chromosome translocations: study of 232 cases originating from 144 families]Y Gillerot, L Koulischer, E Jauniaux
European Journal of Pediatrics|December 1, 1983
Lethal perinatal type II osteogenesis imperfecta in a family with a dominantly inherited type IY Gillerot, J M Druart, L Koulischer
Clinical Genetics|January 1, 1989
Neural tube defects and omphalocele in trisomy 18L van Maldergem, Y Gillerot, L Koulischer
Prenatal Diagnosis|August 1, 1992
Morphological features of a case of retinoic acid embryopathyL Van Maldergem, E Jauniaux, Y Gillerot
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1991
[Amniocentesis and trophoblastic biopsy. Comparison of results]C Gérard, Y Gillerot, L Koulischer, et al.
Pageof 9