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Annales De Genetique
|
January 1, 1982
Translocation 46,X,t(Y;14)(q122;q111) in a case of sterility in the male
P Petit, A Unglik, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1993
Nager acrofacial dysostosis and preaxial polydactyly: a further example with lethal outcome
P Petit, P Moerman, J P Fryns
Annales De Genetique
|
January 1, 1980
Silver staining of the supernumerary chromosome in the cat-eye syndrome
P Petit, S Godart, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1991
Lobar holoprosencephaly and Xq22 deletion
P Petit, P Moerman, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1991
The fetal phenotype of partial trisomy of the long arm of chromosome 4 (4q22----4qter)
P Petit, P Moerman, J P Fryns
Bordeaux Medical
|
April 1, 1970
[Specific serotherapy of envenomization by "Bothrops lanceolatus". 1st therapeutic trials of monovalent serum prepared by Institut Pasteur]
R Mille, C Saint-Cyr, P Petit
American Journal of Medical Genetics
|
February 1, 1992
Acrofacial dysostosis syndrome type Rodriguez: a new lethal MCA syndrome
P Petit, P Moerman, J P Fryns
Clinical Genetics
|
April 1, 1992
Full 69,XXY triploidy and sex-reversal: a further example of true hermaphrodism associated with multiple malformations
P Petit, P Moerman, J P Fryns
Journal De Radiologie
|
January 27, 2005
[Early cholangitis complicating percutaneous biliary drainage]
V Vidal, C S Ho, P Petit
Revue D'Elevage Et De Medecine Veterinaire Des Pays Tropicaux
|
January 1, 1980
[Biochemical polymorphism of hemoglobin in Moroccan cattle populations]
J P Petit, L Mahin, J Briouga
Page
of 40
Search research articles
Search
Showing results (71-80 of 398) with videos related to
Sort By:
Page
of 40
Annales De Genetique
|
January 1, 1982
Translocation 46,X,t(Y;14)(q122;q111) in a case of sterility in the male
P Petit, A Unglik, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1993
Nager acrofacial dysostosis and preaxial polydactyly: a further example with lethal outcome
P Petit, P Moerman, J P Fryns
Annales De Genetique
|
January 1, 1980
Silver staining of the supernumerary chromosome in the cat-eye syndrome
P Petit, S Godart, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1991
Lobar holoprosencephaly and Xq22 deletion
P Petit, P Moerman, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1991
The fetal phenotype of partial trisomy of the long arm of chromosome 4 (4q22----4qter)
P Petit, P Moerman, J P Fryns
Bordeaux Medical
|
April 1, 1970
[Specific serotherapy of envenomization by "Bothrops lanceolatus". 1st therapeutic trials of monovalent serum prepared by Institut Pasteur]
R Mille, C Saint-Cyr, P Petit
American Journal of Medical Genetics
|
February 1, 1992
Acrofacial dysostosis syndrome type Rodriguez: a new lethal MCA syndrome
P Petit, P Moerman, J P Fryns
Clinical Genetics
|
April 1, 1992
Full 69,XXY triploidy and sex-reversal: a further example of true hermaphrodism associated with multiple malformations
P Petit, P Moerman, J P Fryns
Journal De Radiologie
|
January 27, 2005
[Early cholangitis complicating percutaneous biliary drainage]
V Vidal, C S Ho, P Petit
Revue D'Elevage Et De Medecine Veterinaire Des Pays Tropicaux
|
January 1, 1980
[Biochemical polymorphism of hemoglobin in Moroccan cattle populations]
J P Petit, L Mahin, J Briouga
Page
of 40