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A Verloes

Showing results (21-30 of 206) with videos related to

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American Journal of Medical Genetics|March 1, 1992
Lumping of CFC and Baraitser-Patton Noonan-like syndromesA Verloes, M Le Merrer
Annales De Cardiologie Et D'Angeiologie|January 31, 2003
[Aorto-pulmonary collaterals in an infant with 22q11 monosomy]M M Massin, A Verloes
American Journal of Medical Genetics|January 1, 1989
GOMBO syndrome of growth retardation, ocular abnormalities, microcephaly, brachydactyly, and oligophrenia: a possible "new" recessively inherited MCA/MR syndromeA Verloes, J Delfortrie, C Lambotte
Revue Medicale De Liege|February 3, 1999
[Genetic aspects of the 46, XX male]F Marquet, A Beckers, A Verloes
Prenatal Diagnosis|December 1, 1992
Non-radioactive assay of AFP, hCG, and uE3 from dried blood specimens: a low-cost alternative for maternal screening for trisomy 21A Verloes, R Schoos, L Koulischer
Revue Medicale De Liege|November 15, 1987
[The fragile X syndrome in 1987. Recent findings and review of the problem]A Verloes, J Frederic, C Lambotte
Journal De Genetique Humaine|December 1, 1987
Nager acrofacial dysostosis with cleft lipA Verloes, C Foret, C Lambotte
Revue Medicale De Liege|July 8, 1999
[Genetic counseling and prenatal diagnosis]S Lesenfants, A Verloes, L Koulischer
American Journal of Medical Genetics|March 1, 1996
Child with manifestations of Nager acrofacial dysostosis, and the MURCS, VACTERL, and pulmonary agenesis associations: complex defect of blastogenesis?A David, J Mercier, A Verloes
Presse Medicale (Paris, France : 1983)|October 18, 1986
[Typical hydantoin syndrome in a child of a non-epileptic mother]A Verloes, G Pierquin, C Lambotte
Pageof 21

Showing results (21-30 of 206) with videos related to

Sort By:
Pageof 21
American Journal of Medical Genetics|March 1, 1992
Lumping of CFC and Baraitser-Patton Noonan-like syndromesA Verloes, M Le Merrer
Annales De Cardiologie Et D'Angeiologie|January 31, 2003
[Aorto-pulmonary collaterals in an infant with 22q11 monosomy]M M Massin, A Verloes
American Journal of Medical Genetics|January 1, 1989
GOMBO syndrome of growth retardation, ocular abnormalities, microcephaly, brachydactyly, and oligophrenia: a possible "new" recessively inherited MCA/MR syndromeA Verloes, J Delfortrie, C Lambotte
Revue Medicale De Liege|February 3, 1999
[Genetic aspects of the 46, XX male]F Marquet, A Beckers, A Verloes
Prenatal Diagnosis|December 1, 1992
Non-radioactive assay of AFP, hCG, and uE3 from dried blood specimens: a low-cost alternative for maternal screening for trisomy 21A Verloes, R Schoos, L Koulischer
Revue Medicale De Liege|November 15, 1987
[The fragile X syndrome in 1987. Recent findings and review of the problem]A Verloes, J Frederic, C Lambotte
Journal De Genetique Humaine|December 1, 1987
Nager acrofacial dysostosis with cleft lipA Verloes, C Foret, C Lambotte
Revue Medicale De Liege|July 8, 1999
[Genetic counseling and prenatal diagnosis]S Lesenfants, A Verloes, L Koulischer
American Journal of Medical Genetics|March 1, 1996
Child with manifestations of Nager acrofacial dysostosis, and the MURCS, VACTERL, and pulmonary agenesis associations: complex defect of blastogenesis?A David, J Mercier, A Verloes
Presse Medicale (Paris, France : 1983)|October 18, 1986
[Typical hydantoin syndrome in a child of a non-epileptic mother]A Verloes, G Pierquin, C Lambotte
Pageof 21