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U Froster-Iskenius

Showing results (21-30 of 34) with videos related to

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Zentralblatt Fur Gynakologie|January 1, 1988
[Puncture of the chorionic villi. Technic--experiences--risks]U Froster-Iskenius, F Klink, G Grzejszczyk, et al.
The Quarterly Journal of Medicine|October 1, 1988
Molecular analysis of the fragile X syndromeU Froster-Iskenius, M N Patterson, M V Bell, et al.
American Journal of Medical Genetics|January 1, 1986
Normal male carriers in the fra(X) form of X-linked mental retardation (Martin-Bell syndrome)U Froster-Iskenius, B C McGillivray, F J Dill, et al.
European Journal of Pediatrics|August 1, 1984
Hereditary branchial arch defects in a Turkish familyF Aksu, H B von Stockhausen, W Wiebicke, et al.
Prenatal Diagnosis|January 1, 1987
First trimester diagnosis of Rho (D) with an immunofluorescence technique after chorionic villus samplingH C Fuhrman, F Klink, G Grzejszczyk, et al.
Clinical Genetics|March 1, 1987
Roberts syndrome and SC phocomelia. A single genetic entityC Römke, U Froster-Iskenius, K Heyne, et al.
American Journal of Human Genetics|May 1, 1989
An intronic region within the human factor VIII gene is duplicated within Xq28 and is homologous to the polymorphic locus DXS115 (767)M Patterson, J Gitschier, J Bloomfield, et al.
Clinical Genetics|July 1, 1986
Dermatoglyphic peculiarities in families with X-linked mental retardation and fragile site Xq27: a collaborative studyA Rodewald, U Froster-Iskenius, E Käb, et al.
Prenatal Diagnosis|August 1, 1991
Early prenatal diagnosis of the fragile site at Xq27.3 associated with Martin-Bell syndromeN Tommerup, F Søndergaard, A Hanauer, et al.
Nucleic Acids Research|August 25, 1991
Molecular heterogeneity of the fragile X syndromeY Nakahori, S J Knight, J Holland, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Zentralblatt Fur Gynakologie|January 1, 1988
[Puncture of the chorionic villi. Technic--experiences--risks]U Froster-Iskenius, F Klink, G Grzejszczyk, et al.
The Quarterly Journal of Medicine|October 1, 1988
Molecular analysis of the fragile X syndromeU Froster-Iskenius, M N Patterson, M V Bell, et al.
American Journal of Medical Genetics|January 1, 1986
Normal male carriers in the fra(X) form of X-linked mental retardation (Martin-Bell syndrome)U Froster-Iskenius, B C McGillivray, F J Dill, et al.
European Journal of Pediatrics|August 1, 1984
Hereditary branchial arch defects in a Turkish familyF Aksu, H B von Stockhausen, W Wiebicke, et al.
Prenatal Diagnosis|January 1, 1987
First trimester diagnosis of Rho (D) with an immunofluorescence technique after chorionic villus samplingH C Fuhrman, F Klink, G Grzejszczyk, et al.
Clinical Genetics|March 1, 1987
Roberts syndrome and SC phocomelia. A single genetic entityC Römke, U Froster-Iskenius, K Heyne, et al.
American Journal of Human Genetics|May 1, 1989
An intronic region within the human factor VIII gene is duplicated within Xq28 and is homologous to the polymorphic locus DXS115 (767)M Patterson, J Gitschier, J Bloomfield, et al.
Clinical Genetics|July 1, 1986
Dermatoglyphic peculiarities in families with X-linked mental retardation and fragile site Xq27: a collaborative studyA Rodewald, U Froster-Iskenius, E Käb, et al.
Prenatal Diagnosis|August 1, 1991
Early prenatal diagnosis of the fragile site at Xq27.3 associated with Martin-Bell syndromeN Tommerup, F Søndergaard, A Hanauer, et al.
Nucleic Acids Research|August 25, 1991
Molecular heterogeneity of the fragile X syndromeY Nakahori, S J Knight, J Holland, et al.
Pageof 4