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Thyroid : Official Journal of the American Thyroid Association|February 1, 1997
Resistance to thyroid hormone in a family caused by a new point mutation L330S in the thyroid receptor (TR) beta geneJ Pohlenz, G Wildhardt, B Zabel, et al.Human Genetics|February 1, 1991
No evidence for sequences structurally related to the RB1 gene in the human genomeC Belka, V Greger, B Zabel, et al.Human Genetics|April 1, 1995
Non-radioactive multiplex-SSCP analysis: detection of a new type II procollagen gene (COL2A1) mutationA Winterpacht, K Hilbert, U Schwarze, et al.Human Genetics|August 1, 1997
Human fibroblast growth factor receptor 3 gene (FGFR3): genomic sequence and primer set information for gene analysisC Wüchner, K Hilbert, B Zabel, et al.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|April 1, 1991
[Hepatitis B virus DNA. Current diagnosis in children with chronic hepatitis B]S Wirth, K M Keller, W Baumann, et al.American Journal of Medical Genetics. Part A|February 11, 2005
Escobar variant with pursed mouth, creased tongue, ophthalmologic features, and scoliosis in 6 children from OmanAnna Rajab, K Hoffmann, A Ganesh, et al.Genomics|March 10, 2000
Mapping and structure of DMXL1, a human homologue of the DmX gene from Drosophila melanogaster coding for a WD repeat proteinC Kraemer, T Enklaar, B Zabel, et al.Human Genetics|April 7, 1977
A girl with partial long-arm deletion of chromosome 11 and familial pericentric inversion of chromosome 9B Zabel, S Hansen, U Hilig, et al.Journal of Pediatric Gastroenterology and Nutrition|May 1, 1992
Hepatitis B virus DNA in liver tissue of chronic HBsAg carriers in childhood and its relationship to other viral markersS Wirth, K M Keller, E Schaefer, et al.Human Genetics|June 10, 1977
Short-arm deletion of an X chromosome (45,XO/46,XX p--)P Kaiser, K Gerhard-Ratschow, B Zabel, et al.Pageof 18