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Journal De Genetique Humaine
|
December 1, 1983
[Anhidrotic ectodermal dysplasia (apropos of 3 families). Abnormal hair, a sign of heterozygosity?]
B Le Marec, M Roussey, J Chevrant-Breton, et al.
Annales De Genetique
|
January 1, 1985
[Trisomy 20p derived from a maternal pericentric inversion and brachymesophalangy of the index finger]
J Lucas, F Le Mée, B Le Marec, et al.
Annales De Genetique
|
January 1, 1986
46,XX,t(15;21)/47,XX,15p-,+21 mosaicism in a child with Down's syndrome
J Lucas, F Le Mee, K Pluquailec, et al.
Human Genetics
|
December 1, 1991
Oto-palato-digital syndrome type I: further evidence for assignment of the locus to Xq28
V Biancalana, B Le Marec, S Odent, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 1, 1986
[Anencephaly and diprosopy: 2 cases]
H Journel, P Parent, H Leguern, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 1, 1980
[Late prenatal diagnosis of fetal growth retardation: the diagnosis of a case of trisomy 18 (author's transl)]
B Le Marec, G Defawe, J E Mention, et al.
Archives Francaises De Pediatrie
|
January 1, 1988
[Stenosis of the common bile duct on a common biliopancreatic duct]
A Dabadie, M Roussey, B Fremond, et al.
European Journal of Human Genetics : EJHG
|
October 20, 2000
A new mutation in the six-domain of SIX3 gene causes holoprosencephaly
L Pasquier, C Dubourg, M Blayau, et al.
Journal De Genetique Humaine
|
October 1, 1979
[Recessive microencephaly linked to the X chromosome]
Y Deshaies, H D Rott, H F Wissmuller, et al.
Presse Medicale (Paris, France : 1983)
|
September 13, 1986
[Genetic counseling in cancerology]
B Le Marec, E Le Gall, H Journel, et al.
Page
of 11
Search research articles
Search
Showing results (41-50 of 103) with videos related to
Sort By:
Page
of 11
Journal De Genetique Humaine
|
December 1, 1983
[Anhidrotic ectodermal dysplasia (apropos of 3 families). Abnormal hair, a sign of heterozygosity?]
B Le Marec, M Roussey, J Chevrant-Breton, et al.
Annales De Genetique
|
January 1, 1985
[Trisomy 20p derived from a maternal pericentric inversion and brachymesophalangy of the index finger]
J Lucas, F Le Mée, B Le Marec, et al.
Annales De Genetique
|
January 1, 1986
46,XX,t(15;21)/47,XX,15p-,+21 mosaicism in a child with Down's syndrome
J Lucas, F Le Mee, K Pluquailec, et al.
Human Genetics
|
December 1, 1991
Oto-palato-digital syndrome type I: further evidence for assignment of the locus to Xq28
V Biancalana, B Le Marec, S Odent, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 1, 1986
[Anencephaly and diprosopy: 2 cases]
H Journel, P Parent, H Leguern, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 1, 1980
[Late prenatal diagnosis of fetal growth retardation: the diagnosis of a case of trisomy 18 (author's transl)]
B Le Marec, G Defawe, J E Mention, et al.
Archives Francaises De Pediatrie
|
January 1, 1988
[Stenosis of the common bile duct on a common biliopancreatic duct]
A Dabadie, M Roussey, B Fremond, et al.
European Journal of Human Genetics : EJHG
|
October 20, 2000
A new mutation in the six-domain of SIX3 gene causes holoprosencephaly
L Pasquier, C Dubourg, M Blayau, et al.
Journal De Genetique Humaine
|
October 1, 1979
[Recessive microencephaly linked to the X chromosome]
Y Deshaies, H D Rott, H F Wissmuller, et al.
Presse Medicale (Paris, France : 1983)
|
September 13, 1986
[Genetic counseling in cancerology]
B Le Marec, E Le Gall, H Journel, et al.
Page
of 11