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Archives Francaises De Pediatrie
|
April 1, 1972
[Familial condensing osteopathy with leontiasis ossium]
R Bernard, F Giraud, J F Mattéi
Prenatal Diagnosis
|
February 1, 1989
Physicians' acceptability of termination of pregnancy after prenatal diagnosis in southern France
C Julian, P Huard, J Gouvernet, et al.
Nouvelle Revue Francaise D'Hematologie; Blood Cells
|
January 1, 1977
[Acquired idiopathic sideroblastic anemia: three cases with the same supplemental chromosome marker (47 Mar+)]
J F Dor, J F Mattéi, M G Mattéi, et al.
Archives Francaises De Pediatrie
|
April 1, 1979
[Partial trisomy 21]
J F Mattéi, M G Mattéi, J P Ardissone, et al.
Nature Genetics
|
April 1, 1996
XNP mutation in a large family with Juberg-Marsidi syndrome
L Villard, J Gecz, J F Mattéi, et al.
Archives Francaises De Pediatrie
|
June 1, 1978
[Upper extremity abnormalities, thrombopenia and thrombopathy. 3 cases]
D Thévenieau, J F Mattéi, I Juhan, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 1, 1990
[The usefulness of the level of alpha-fetoprotein (AFP) and electrophoresis of amniotic acetylcholinesterase for the detection of selected congenital malformations]
M C Lemonnier, C Julian, S Aymé, et al.
European Journal of Human Genetics : EJHG
|
April 26, 2000
Prenatal detection of a 17p11.2 duplication resulting from a rare recombination event and novel PCR-based strategy for molecular identification of Charcot-Marie-Tooth disease type 1A
R Bernard, V Labelle, P Negre, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 1, 1986
Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers
I Oberlé, R Heilig, J P Moisan, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Archives Francaises De Pediatrie
|
April 1, 1972
[Familial condensing osteopathy with leontiasis ossium]
R Bernard, F Giraud, J F Mattéi
Prenatal Diagnosis
|
February 1, 1989
Physicians' acceptability of termination of pregnancy after prenatal diagnosis in southern France
C Julian, P Huard, J Gouvernet, et al.
Nouvelle Revue Francaise D'Hematologie; Blood Cells
|
January 1, 1977
[Acquired idiopathic sideroblastic anemia: three cases with the same supplemental chromosome marker (47 Mar+)]
J F Dor, J F Mattéi, M G Mattéi, et al.
Archives Francaises De Pediatrie
|
April 1, 1979
[Partial trisomy 21]
J F Mattéi, M G Mattéi, J P Ardissone, et al.
Nature Genetics
|
April 1, 1996
XNP mutation in a large family with Juberg-Marsidi syndrome
L Villard, J Gecz, J F Mattéi, et al.
Archives Francaises De Pediatrie
|
June 1, 1978
[Upper extremity abnormalities, thrombopenia and thrombopathy. 3 cases]
D Thévenieau, J F Mattéi, I Juhan, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 1, 1990
[The usefulness of the level of alpha-fetoprotein (AFP) and electrophoresis of amniotic acetylcholinesterase for the detection of selected congenital malformations]
M C Lemonnier, C Julian, S Aymé, et al.
European Journal of Human Genetics : EJHG
|
April 26, 2000
Prenatal detection of a 17p11.2 duplication resulting from a rare recombination event and novel PCR-based strategy for molecular identification of Charcot-Marie-Tooth disease type 1A
R Bernard, V Labelle, P Negre, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 1, 1986
Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers
I Oberlé, R Heilig, J P Moisan, et al.
Page
of 1