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Annales D'Oto-Laryngologie Et De Chirurgie Cervico Faciale : Bulletin De La Societe D'Oto-Laryngologie Des Hopitaux De Paris
|
January 1, 1983
[2 uncommon malformations of the nose. Attempt at an explanation]
M J Ployet, B Loustalot, C Moraine, et al.
American Journal of Medical Genetics
|
August 17, 1999
Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndrome
S Briault, S Odent, J Lucas, et al.
Acta Neuropathologica
|
January 1, 1995
Developmental aspects of type II lissencephaly. Comparative study of dysplastic lesions in fetal and post-natal brains
A Gelot, T Billette de Villemeur, C Bordarier, et al.
Journal of Medical Genetics
|
February 1, 1988
Lethal acrodysgenital dwarfism: a severe lethal condition resembling Smith-Lemli-Opitz syndrome
M L Merrer, M L Briard, S Girard, et al.
Revue D'Oto-Neuro-Ophtalmologie
|
March 1, 1983
[A rare cephalic malformation : craniostenosis with hemiarhinia. Pathogenetic discussion and therapeutic problems]
B Loustalot, M J Ployet, M P Delplace, et al.
Journal De Genetique Humaine
|
November 1, 1976
[Familial blepharophimosis and female sterility: pleiotropism or linked genes?]
C Moraine, C Titeca, M P Delplace, et al.
Annales De Dermatologie Et De Venereologie
|
January 1, 1984
[Albright's hereditary osteodystrophy with multiple cutaneous osteomas]
G Lorette, J P Valat, P Gatti, et al.
Archives Francaises De Pediatrie
|
August 1, 1988
[Lethal syndromes with thin bones]
P Maroteaux, L Cohen-Solal, J Bonaventure, et al.
Annales De Genetique
|
January 1, 1984
[Association of VACTERL and hydrocephalus: a new familial entity]
M L Briard, M le Merrer, H Plauchu, et al.
Prenatal Diagnosis
|
August 1, 1995
Prenatal diagnosis of trisomy 8 mosaicism in CVS after abnormal ultrasound findings at 12 weeks
A Guichet, S Briault, A Toutain, et al.
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Search research articles
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Showing results (41-50 of 94) with videos related to
Sort By:
Page
of 10
Annales D'Oto-Laryngologie Et De Chirurgie Cervico Faciale : Bulletin De La Societe D'Oto-Laryngologie Des Hopitaux De Paris
|
January 1, 1983
[2 uncommon malformations of the nose. Attempt at an explanation]
M J Ployet, B Loustalot, C Moraine, et al.
American Journal of Medical Genetics
|
August 17, 1999
Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndrome
S Briault, S Odent, J Lucas, et al.
Acta Neuropathologica
|
January 1, 1995
Developmental aspects of type II lissencephaly. Comparative study of dysplastic lesions in fetal and post-natal brains
A Gelot, T Billette de Villemeur, C Bordarier, et al.
Journal of Medical Genetics
|
February 1, 1988
Lethal acrodysgenital dwarfism: a severe lethal condition resembling Smith-Lemli-Opitz syndrome
M L Merrer, M L Briard, S Girard, et al.
Revue D'Oto-Neuro-Ophtalmologie
|
March 1, 1983
[A rare cephalic malformation : craniostenosis with hemiarhinia. Pathogenetic discussion and therapeutic problems]
B Loustalot, M J Ployet, M P Delplace, et al.
Journal De Genetique Humaine
|
November 1, 1976
[Familial blepharophimosis and female sterility: pleiotropism or linked genes?]
C Moraine, C Titeca, M P Delplace, et al.
Annales De Dermatologie Et De Venereologie
|
January 1, 1984
[Albright's hereditary osteodystrophy with multiple cutaneous osteomas]
G Lorette, J P Valat, P Gatti, et al.
Archives Francaises De Pediatrie
|
August 1, 1988
[Lethal syndromes with thin bones]
P Maroteaux, L Cohen-Solal, J Bonaventure, et al.
Annales De Genetique
|
January 1, 1984
[Association of VACTERL and hydrocephalus: a new familial entity]
M L Briard, M le Merrer, H Plauchu, et al.
Prenatal Diagnosis
|
August 1, 1995
Prenatal diagnosis of trisomy 8 mosaicism in CVS after abnormal ultrasound findings at 12 weeks
A Guichet, S Briault, A Toutain, et al.
Page
of 10