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Pediatrie
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January 1, 1987
[Keratosis follicularis decalvans: nosological discussion of Siemens' disease. Apropos of 3 cases]
G Guillet, F Labouche, F Cambazard, et al.
Revue Des Maladies Respiratoires
|
January 1, 1989
[Mucoviscidosis: current diagnostic possibilities. Applications in perinatology]
C Ferec, J J Chabaud, P Parent, et al.
American Journal of Medical Genetics. Part A
|
August 7, 2007
18p trisomy: a case of direct 18p duplication characterized by molecular cytogenetic analysis
H Marical, M J Le Bris, N Douet-Guilbert, et al.
Prenatal Diagnosis
|
June 1, 1990
Prenatal diagnosis of del(15)(q11q13)
M J Le Bris-Quillevere, D Riviere, E Pluchon-Riviere, et al.
Clinical Neuropathology
|
July 22, 2005
Fetal aqueductal glioneuronal hamartoma: a clinicopathological and physiopathological study of three cases
P Marcorelles, C Fallet-Bianco, J F Oury, et al.
Archives Francaises De Pediatrie
|
October 1, 1988
[Approaching the gene of mucoviscidosis. New data]
C Ferec, J F Morin, P Parent, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 1, 1995
[Clinical heterogeneity of Townes-Brocks syndrome]
P Parent, M Bensaid, H Le Guern, et al.
Journal De Genetique Humaine
|
January 1, 1987
[What course should be adopted after the discovery of a gonosome anomaly in the fetal karyotype?]
B Le Marec, L Larget-Piet, A Larget-Piet, et al.
Nature Genetics
|
April 1, 1994
A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12
D Bonnet, A Pelet, L Legeai-Mallet, et al.
Journal of Hazardous Materials
|
March 1, 2022
KI and TEDA influences towards the retention of radiotoxic CH<sub>3</sub>I by activated carbons
H Lin, M Chebbi, C Monsanglant-Louvet, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 86) with videos related to
Sort By:
Page
of 9
Pediatrie
|
January 1, 1987
[Keratosis follicularis decalvans: nosological discussion of Siemens' disease. Apropos of 3 cases]
G Guillet, F Labouche, F Cambazard, et al.
Revue Des Maladies Respiratoires
|
January 1, 1989
[Mucoviscidosis: current diagnostic possibilities. Applications in perinatology]
C Ferec, J J Chabaud, P Parent, et al.
American Journal of Medical Genetics. Part A
|
August 7, 2007
18p trisomy: a case of direct 18p duplication characterized by molecular cytogenetic analysis
H Marical, M J Le Bris, N Douet-Guilbert, et al.
Prenatal Diagnosis
|
June 1, 1990
Prenatal diagnosis of del(15)(q11q13)
M J Le Bris-Quillevere, D Riviere, E Pluchon-Riviere, et al.
Clinical Neuropathology
|
July 22, 2005
Fetal aqueductal glioneuronal hamartoma: a clinicopathological and physiopathological study of three cases
P Marcorelles, C Fallet-Bianco, J F Oury, et al.
Archives Francaises De Pediatrie
|
October 1, 1988
[Approaching the gene of mucoviscidosis. New data]
C Ferec, J F Morin, P Parent, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 1, 1995
[Clinical heterogeneity of Townes-Brocks syndrome]
P Parent, M Bensaid, H Le Guern, et al.
Journal De Genetique Humaine
|
January 1, 1987
[What course should be adopted after the discovery of a gonosome anomaly in the fetal karyotype?]
B Le Marec, L Larget-Piet, A Larget-Piet, et al.
Nature Genetics
|
April 1, 1994
A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12
D Bonnet, A Pelet, L Legeai-Mallet, et al.
Journal of Hazardous Materials
|
March 1, 2022
KI and TEDA influences towards the retention of radiotoxic CH<sub>3</sub>I by activated carbons
H Lin, M Chebbi, C Monsanglant-Louvet, et al.
Page
of 9