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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 I
Y Gillerot, J M Druart, L Koulischer
Clinical Genetics
|
January 1, 1989
Neural tube defects and omphalocele in trisomy 18
L van Maldergem, Y Gillerot, L Koulischer
Prenatal Diagnosis
|
August 1, 1992
Morphological features of a case of retinoic acid embryopathy
L 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.
Page
of 9
Search research articles
Search
Showing results (11-20 of 87) with videos related to
Sort By:
Page
of 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 I
Y Gillerot, J M Druart, L Koulischer
Clinical Genetics
|
January 1, 1989
Neural tube defects and omphalocele in trisomy 18
L van Maldergem, Y Gillerot, L Koulischer
Prenatal Diagnosis
|
August 1, 1992
Morphological features of a case of retinoic acid embryopathy
L 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.
Page
of 9