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G Tariverdian

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

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Brain & Development|January 1, 1990
Follow-up of monozygotic twins concordant for the Rett syndromeG Tariverdian
Cytogenetics and Cell Genetics|February 15, 2001
Some problems in the genetics of X-linked mental retardationG Tariverdian, F Vogel
Human Genetics|January 1, 1982
Nonspecific X-linked mental retardation--a reviewG Tariverdian, B Weck
Clinical Genetics|April 1, 1995
Symptomatic heterozygosity in the Ellis-van Creveld syndrome?S Spranger, G Tariverdian
Human Genetics|January 1, 1987
A monozygotic twin pair with Rett syndromeG Tariverdian, G Kantner, F Vogel
Human Genetics|December 1, 1987
Prenatal enzymatic diagnosis and exclusion of Krabbe's disease (globoid-cell leukodystrophy) using chorionic villi in five risk pregnanciesK Harzer, H D Hager, G Tariverdian
American Journal of Medical Genetics|November 1, 1991
Tapetoretinal degeneration in brothers with apparent Cohen syndrome: nosology with Mirhosseini-Holmes-Walton syndromeO Steinlein, G Tariverdian, H U Boll, et al.
Human Genetics|April 1, 1988
The secretor locus as a marker for prenatal prediction of myotonic dystrophy (DM)J Greiner, D H Spengler, J Krüger, et al.
American Journal of Medical Genetics|February 1, 1991
Mental retardation, acromegalic face, and megalotestes in two half-brothers: a specific form of X-linked mental retardation without fra(X) (q)?G Tariverdian, U Froster-Iskenius, G Deuschl, et al.
American Journal of Medical Genetics|March 17, 2001
Misclassification risk of patients with bilateral cleft lip and palate and manifestations of median facial dysplasia: A new variant of del(22q11.2) syndrome?B R Schulze, G Tariverdian, G Komposch, et al.
Pageof 3

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

Sort By:
Pageof 3
Brain & Development|January 1, 1990
Follow-up of monozygotic twins concordant for the Rett syndromeG Tariverdian
Cytogenetics and Cell Genetics|February 15, 2001
Some problems in the genetics of X-linked mental retardationG Tariverdian, F Vogel
Human Genetics|January 1, 1982
Nonspecific X-linked mental retardation--a reviewG Tariverdian, B Weck
Clinical Genetics|April 1, 1995
Symptomatic heterozygosity in the Ellis-van Creveld syndrome?S Spranger, G Tariverdian
Human Genetics|January 1, 1987
A monozygotic twin pair with Rett syndromeG Tariverdian, G Kantner, F Vogel
Human Genetics|December 1, 1987
Prenatal enzymatic diagnosis and exclusion of Krabbe's disease (globoid-cell leukodystrophy) using chorionic villi in five risk pregnanciesK Harzer, H D Hager, G Tariverdian
American Journal of Medical Genetics|November 1, 1991
Tapetoretinal degeneration in brothers with apparent Cohen syndrome: nosology with Mirhosseini-Holmes-Walton syndromeO Steinlein, G Tariverdian, H U Boll, et al.
Human Genetics|April 1, 1988
The secretor locus as a marker for prenatal prediction of myotonic dystrophy (DM)J Greiner, D H Spengler, J Krüger, et al.
American Journal of Medical Genetics|February 1, 1991
Mental retardation, acromegalic face, and megalotestes in two half-brothers: a specific form of X-linked mental retardation without fra(X) (q)?G Tariverdian, U Froster-Iskenius, G Deuschl, et al.
American Journal of Medical Genetics|March 17, 2001
Misclassification risk of patients with bilateral cleft lip and palate and manifestations of median facial dysplasia: A new variant of del(22q11.2) syndrome?B R Schulze, G Tariverdian, G Komposch, et al.
Pageof 3