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M Ioan

Showing results (1-10 of 30) with videos related to

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Ftiziologia|July 1, 1971
[Studies of bacterial flora in pulmonary suppurations, using pulmonary aspirative punctures]M Ioan, A Vlad
Romanian Journal of Endocrinology|January 1, 1993
Is non-invasive diagnosis possible in Down's syndrome?D M Ioan, R Lăpădat
Endocrinologie|January 1, 1991
Trisomy 4p--a new case of congenital myxedemaD M Ioan, T Ghitan
Revista Medico-Chirurgicala a Societatii De Medici Si Naturalisti Din Iasi|January 1, 1970
[Mucopolysaccharides of the digestive tract in common laboratory animals. Mucopolysaccharides of the intestinal segment]G Adomnicăi, M Ioan, G Mihalache
Genetic Counseling (Geneva, Switzerland)|May 23, 2007
Kabuki syndrome: description of a 2-year old Roumanian boy and review of the literatureD M Ioan, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 24, 2004
Floating-Harbor syndrome in two sisters: autosomal recessive inheritance or germinal mosaicism?D M Ioan, J P Fryns
Genetic Counseling (Geneva, Switzerland)|November 6, 2002
Costello syndrome in two siblings and minor manifestations in their mother. Further evidence for autosomal dominant inheritance?D M Ioan, J P Fryns
Endocrinologie|July 1, 1989
Microcytogenetics of chromosome XD M Ioan, D Ghergar, T Pop
Genetic Counseling (Geneva, Switzerland)|January 31, 2006
Terminal distal 13q trisomy due to de novo dup(13)(q32 --> qter)D M Ioan, J Vermeesch, J P Fryns
Genetic Counseling (Geneva, Switzerland)|August 2, 2002
Oculo-dento-digital dysplasia (OMIM *164200). Full manifestation of the syndrome in a 9.5 year-old girl and type III syndactyly in the fatherD M Ioan, D Dagomiz, J P Fryns
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Ftiziologia|July 1, 1971
[Studies of bacterial flora in pulmonary suppurations, using pulmonary aspirative punctures]M Ioan, A Vlad
Romanian Journal of Endocrinology|January 1, 1993
Is non-invasive diagnosis possible in Down's syndrome?D M Ioan, R Lăpădat
Endocrinologie|January 1, 1991
Trisomy 4p--a new case of congenital myxedemaD M Ioan, T Ghitan
Revista Medico-Chirurgicala a Societatii De Medici Si Naturalisti Din Iasi|January 1, 1970
[Mucopolysaccharides of the digestive tract in common laboratory animals. Mucopolysaccharides of the intestinal segment]G Adomnicăi, M Ioan, G Mihalache
Genetic Counseling (Geneva, Switzerland)|May 23, 2007
Kabuki syndrome: description of a 2-year old Roumanian boy and review of the literatureD M Ioan, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 24, 2004
Floating-Harbor syndrome in two sisters: autosomal recessive inheritance or germinal mosaicism?D M Ioan, J P Fryns
Genetic Counseling (Geneva, Switzerland)|November 6, 2002
Costello syndrome in two siblings and minor manifestations in their mother. Further evidence for autosomal dominant inheritance?D M Ioan, J P Fryns
Endocrinologie|July 1, 1989
Microcytogenetics of chromosome XD M Ioan, D Ghergar, T Pop
Genetic Counseling (Geneva, Switzerland)|January 31, 2006
Terminal distal 13q trisomy due to de novo dup(13)(q32 --> qter)D M Ioan, J Vermeesch, J P Fryns
Genetic Counseling (Geneva, Switzerland)|August 2, 2002
Oculo-dento-digital dysplasia (OMIM *164200). Full manifestation of the syndrome in a 9.5 year-old girl and type III syndactyly in the fatherD M Ioan, D Dagomiz, J P Fryns
Pageof 3