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G Tariverdian

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

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Geburtshilfe Und Frauenheilkunde|June 1, 1990
[Early amniocentesis]J Klapp, K H Nicolaides, H D Hager, et al.
American Journal of Medical Genetics|August 9, 1996
Severe mental retardation and macroorchidism without mutation in the FMR1 geneE Reyniers, G Wolff, G Tariverdian, et al.
American Journal of Medical Genetics|May 8, 1999
Léri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3S Spranger, S Schiller, A Jauch, et al.
Genomics|June 1, 1997
Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetusesA M Riesewijk, L Hu, U Schulz, et al.
Pathologica|October 17, 1998
Wolf-Hirschhorn syndrome: case report and review of the chromosomal aberrations associated with diaphragmatic defectsC Sergi, B R Schulze, H D Hager, et al.
Pediatric Radiology|April 27, 2001
Ellis-van Creveld syndrome: a generalized dysplasia of enchondral ossificationC Sergi, T Voigtländer, S Zoubaa, et al.
Human Genetics|November 1, 1993
Molecular analysis of mutations in the gene FMR-1 segregating in fragile X familiesP Steinbach, D Wöhrle, G Tariverdian, et al.
Human Genetics|September 12, 2000
Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three mentally retarded individualsM Granzow, S Popp, M Keller, et al.
Human Genetics|October 1, 1994
Molecular analysis of aniridia patients for deletions involving the Wilms' tumor geneM Drechsler, E J Meijers-Heijboer, S Schneider, et al.
European Journal of Pediatrics|May 2, 2000
Maternal uniparental disomy 7--review and further delineation of the phenotypeD Kotzot, D Balmer, A Baumer, et al.
Pageof 3

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

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Geburtshilfe Und Frauenheilkunde|June 1, 1990
[Early amniocentesis]J Klapp, K H Nicolaides, H D Hager, et al.
American Journal of Medical Genetics|August 9, 1996
Severe mental retardation and macroorchidism without mutation in the FMR1 geneE Reyniers, G Wolff, G Tariverdian, et al.
American Journal of Medical Genetics|May 8, 1999
Léri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3S Spranger, S Schiller, A Jauch, et al.
Genomics|June 1, 1997
Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetusesA M Riesewijk, L Hu, U Schulz, et al.
Pathologica|October 17, 1998
Wolf-Hirschhorn syndrome: case report and review of the chromosomal aberrations associated with diaphragmatic defectsC Sergi, B R Schulze, H D Hager, et al.
Pediatric Radiology|April 27, 2001
Ellis-van Creveld syndrome: a generalized dysplasia of enchondral ossificationC Sergi, T Voigtländer, S Zoubaa, et al.
Human Genetics|November 1, 1993
Molecular analysis of mutations in the gene FMR-1 segregating in fragile X familiesP Steinbach, D Wöhrle, G Tariverdian, et al.
Human Genetics|September 12, 2000
Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three mentally retarded individualsM Granzow, S Popp, M Keller, et al.
Human Genetics|October 1, 1994
Molecular analysis of aniridia patients for deletions involving the Wilms' tumor geneM Drechsler, E J Meijers-Heijboer, S Schneider, et al.
European Journal of Pediatrics|May 2, 2000
Maternal uniparental disomy 7--review and further delineation of the phenotypeD Kotzot, D Balmer, A Baumer, et al.
Pageof 3