Search research articles
Contact Us
Filters
Showing results (21-30 of 103) with videos related to
Page
of 11
Sort By:
Archives Francaises De Pediatrie
|
July 1, 1979
[Ophthalmologic evaluation at the age of 2 years of newborn infants hospitalized in the neonatology center at Rennes]
J Sénécal, M Roussey, G Defawe, et al.
Annales De Genetique
|
May 4, 2001
Prader-Willi syndrome and polygonosomal abnormalities in males:about a Prader-Willi/47,XYY patient
S Odent, S Taque, J Lucas, et al.
Journal De Genetique Humaine
|
December 1, 1985
[A rare motive for genetic counseling: the risk of leukemia: apropos of a familial form]
B Le Marec, E Le Gall, P Y Le Prise, et al.
Journal of Medical Genetics
|
May 5, 1999
Unusual fan shaped ossification in a female fetus with radiological features of boomerang dysplasia
S Odent, P Loget, B Le Marec, et al.
Annales De Genetique
|
January 1, 1983
[Pure trisomy 13q13-qter caused by aneusomic recombination of a maternal pericentric inversion]
J Lucas, F Le Mée, F Picard, et al.
Pediatrie
|
June 1, 1983
[Association of trisomy 21 and gonosomal trisomy. Apropos of 2 cases]
Y Castel, B Le Marec, L Toudic, et al.
Clinical Genetics
|
May 1, 1977
Heredity of idiopathic haemochromatosis: a study of 106 families
M Simon, J L Alexandre, M Bourel, et al.
Pediatrie
|
September 1, 1985
[Neural tube defects (spina bifida and anencephaly) in Brittany]
H Journel, J Milon, A Dabadie, et al.
Journal De Genetique Humaine
|
January 1, 1989
[Argininosuccinic aciduria. A new case revealed by psychiatric disorders]
S Odent, M Roussey, H Journel, et al.
Journal De Genetique Humaine
|
September 1, 1989
[Truncus arteriosus: an autosomal recessive disease?]
B le Marec, S Odent, C Almange, et al.
Page
of 11
Search research articles
Search
Showing results (21-30 of 103) with videos related to
Sort By:
Page
of 11
Archives Francaises De Pediatrie
|
July 1, 1979
[Ophthalmologic evaluation at the age of 2 years of newborn infants hospitalized in the neonatology center at Rennes]
J Sénécal, M Roussey, G Defawe, et al.
Annales De Genetique
|
May 4, 2001
Prader-Willi syndrome and polygonosomal abnormalities in males:about a Prader-Willi/47,XYY patient
S Odent, S Taque, J Lucas, et al.
Journal De Genetique Humaine
|
December 1, 1985
[A rare motive for genetic counseling: the risk of leukemia: apropos of a familial form]
B Le Marec, E Le Gall, P Y Le Prise, et al.
Journal of Medical Genetics
|
May 5, 1999
Unusual fan shaped ossification in a female fetus with radiological features of boomerang dysplasia
S Odent, P Loget, B Le Marec, et al.
Annales De Genetique
|
January 1, 1983
[Pure trisomy 13q13-qter caused by aneusomic recombination of a maternal pericentric inversion]
J Lucas, F Le Mée, F Picard, et al.
Pediatrie
|
June 1, 1983
[Association of trisomy 21 and gonosomal trisomy. Apropos of 2 cases]
Y Castel, B Le Marec, L Toudic, et al.
Clinical Genetics
|
May 1, 1977
Heredity of idiopathic haemochromatosis: a study of 106 families
M Simon, J L Alexandre, M Bourel, et al.
Pediatrie
|
September 1, 1985
[Neural tube defects (spina bifida and anencephaly) in Brittany]
H Journel, J Milon, A Dabadie, et al.
Journal De Genetique Humaine
|
January 1, 1989
[Argininosuccinic aciduria. A new case revealed by psychiatric disorders]
S Odent, M Roussey, H Journel, et al.
Journal De Genetique Humaine
|
September 1, 1989
[Truncus arteriosus: an autosomal recessive disease?]
B le Marec, S Odent, C Almange, et al.
Page
of 11