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Clinical Genetics
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October 1, 1982
Familial ectrodactyly and polydactyly: variable expressivity of one single gene--embryological considerations
N van Regemorter, J Milaire, J Ramet, et al.
Journal De Genetique Humaine
|
August 1, 1988
Familial trisomy 11p resulting from a balanced paternal translocation: 3 new cases including first trimester diagnosis
G Ogur, F Hayez, A Herinckx, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1992
Lethal malformation syndrome in three siblings. A variable expression of the same entity?
N Van Regemorter, G Pierquin, E Vamos, et al.
American Journal of Medical Genetics
|
September 24, 2002
Neuroimaging fails to identify asymptomatic carriers of familial porencephaly
C Vilain, N Van Regemorter, A Verloes, et al.
Genetic Counseling (Geneva, Switzerland)
|
July 17, 1998
Need for search for cryptic translocation in parents with several children affected with MCA: report of a cryptic translocation (10;14) detected by FISH
D Delneste, E Vamos, G Pierquin, et al.
Radiology
|
July 1, 1982
Measurements of fetal kidney growth on ultrasound
P Jeanty, M Dramaix-Wilmet, N Elkhazen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 1, 1972
[Distribution of two peptides of -aminobutyric acid in human brain and CSF]
N Van Regemorter, Y Mardens, A Lowenthal, et al.
Dermatologica
|
January 1, 1989
Lethal course of X-linked dominant chondrodysplasia punctata in a male newborn
L De Raeve, M Song, G De Dobbeleer, et al.
Acta Paediatrica Belgica
|
April 1, 1981
Major congenital malformations in 5448 newborns: comments on genetic counseling and prenatal diagnosis
N Van Regemorter, J Dodion, C Druart, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
March 24, 2009
[Major alpha-thalassemia: antenatal diagnosis, case report and literature review]
H Saadi, S Alexander, P Barlow, et al.
Page
of 8
Search research articles
Search
Showing results (11-20 of 71) with videos related to
Sort By:
Page
of 8
Clinical Genetics
|
October 1, 1982
Familial ectrodactyly and polydactyly: variable expressivity of one single gene--embryological considerations
N van Regemorter, J Milaire, J Ramet, et al.
Journal De Genetique Humaine
|
August 1, 1988
Familial trisomy 11p resulting from a balanced paternal translocation: 3 new cases including first trimester diagnosis
G Ogur, F Hayez, A Herinckx, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1992
Lethal malformation syndrome in three siblings. A variable expression of the same entity?
N Van Regemorter, G Pierquin, E Vamos, et al.
American Journal of Medical Genetics
|
September 24, 2002
Neuroimaging fails to identify asymptomatic carriers of familial porencephaly
C Vilain, N Van Regemorter, A Verloes, et al.
Genetic Counseling (Geneva, Switzerland)
|
July 17, 1998
Need for search for cryptic translocation in parents with several children affected with MCA: report of a cryptic translocation (10;14) detected by FISH
D Delneste, E Vamos, G Pierquin, et al.
Radiology
|
July 1, 1982
Measurements of fetal kidney growth on ultrasound
P Jeanty, M Dramaix-Wilmet, N Elkhazen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 1, 1972
[Distribution of two peptides of -aminobutyric acid in human brain and CSF]
N Van Regemorter, Y Mardens, A Lowenthal, et al.
Dermatologica
|
January 1, 1989
Lethal course of X-linked dominant chondrodysplasia punctata in a male newborn
L De Raeve, M Song, G De Dobbeleer, et al.
Acta Paediatrica Belgica
|
April 1, 1981
Major congenital malformations in 5448 newborns: comments on genetic counseling and prenatal diagnosis
N Van Regemorter, J Dodion, C Druart, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
March 24, 2009
[Major alpha-thalassemia: antenatal diagnosis, case report and literature review]
H Saadi, S Alexander, P Barlow, et al.
Page
of 8