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E Holinski-Feder

Showing results (1-10 of 39) with videos related to

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MMW Fortschritte Der Medizin|March 6, 2010
[The role of genetic predisposition in early detection of cancer]E Holinski-Feder
Deutsche Medizinische Wochenschrift (1946)|August 8, 2008
[Hereditary nonpolyposis colorectal carcinoma: state of the art]E Holinski-Feder, M Morak
Familial Cancer|March 23, 2020
Analysis of 3297 individuals suggests that the pathogenic germline 5'-UTR variant BRCA1 c.-107A > T is not common in south-east GermanyA Laner, A Benet-Pages, B Neitzel, et al.
Der Nervenarzt|September 19, 2009
[Fragile X-associated tremor/ataxia syndrome]C Finke, R Horváth, E Holinski-Feder, et al.
Clinical Genetics|July 13, 2010
MUTYH-associated polyposis - variability of the clinical phenotype in patients with biallelic and monoallelic MUTYH mutations and report on novel mutationsM Morak, A Laner, U Bacher, et al.
Genomics|February 9, 2000
The SOX8 gene is located within 700 kb of the tip of chromosome 16p and is deleted in a patient with ATR-16 syndromeD Pfeifer, F Poulat, E Holinski-Feder, et al.
Genetic Testing|March 6, 2004
FMR1 gene deletion/reversion: a pitfall of fragile X carrier testingM Gasteiger, E Grasbon-Frodl, B Neitzel, et al.
American Journal of Medical Genetics|July 12, 1996
Regional localization of two MRX genes to Xq28 (MRX28) and to Xp11.4-Xp22.12 (MRX33)E Holinski-Feder, A Golla, I Rost, et al.
Pediatrics|November 14, 1997
Large intergenerational variation in age of onset in two young patients with Huntington's disease presenting as dyskinesiaE Holinski-Feder, K B Jedele, K Hörtnagel, et al.
Clinical Genetics|October 7, 1998
Spinal and bulbar muscular atrophy (SBMA): somatic stability of an expanded CAG repeat in fetal tissuesK B Jedele, D Wahl, S Chahrokh-Zadeh, et al.
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
MMW Fortschritte Der Medizin|March 6, 2010
[The role of genetic predisposition in early detection of cancer]E Holinski-Feder
Deutsche Medizinische Wochenschrift (1946)|August 8, 2008
[Hereditary nonpolyposis colorectal carcinoma: state of the art]E Holinski-Feder, M Morak
Familial Cancer|March 23, 2020
Analysis of 3297 individuals suggests that the pathogenic germline 5'-UTR variant BRCA1 c.-107A > T is not common in south-east GermanyA Laner, A Benet-Pages, B Neitzel, et al.
Der Nervenarzt|September 19, 2009
[Fragile X-associated tremor/ataxia syndrome]C Finke, R Horváth, E Holinski-Feder, et al.
Clinical Genetics|July 13, 2010
MUTYH-associated polyposis - variability of the clinical phenotype in patients with biallelic and monoallelic MUTYH mutations and report on novel mutationsM Morak, A Laner, U Bacher, et al.
Genomics|February 9, 2000
The SOX8 gene is located within 700 kb of the tip of chromosome 16p and is deleted in a patient with ATR-16 syndromeD Pfeifer, F Poulat, E Holinski-Feder, et al.
Genetic Testing|March 6, 2004
FMR1 gene deletion/reversion: a pitfall of fragile X carrier testingM Gasteiger, E Grasbon-Frodl, B Neitzel, et al.
American Journal of Medical Genetics|July 12, 1996
Regional localization of two MRX genes to Xq28 (MRX28) and to Xp11.4-Xp22.12 (MRX33)E Holinski-Feder, A Golla, I Rost, et al.
Pediatrics|November 14, 1997
Large intergenerational variation in age of onset in two young patients with Huntington's disease presenting as dyskinesiaE Holinski-Feder, K B Jedele, K Hörtnagel, et al.
Clinical Genetics|October 7, 1998
Spinal and bulbar muscular atrophy (SBMA): somatic stability of an expanded CAG repeat in fetal tissuesK B Jedele, D Wahl, S Chahrokh-Zadeh, et al.
Pageof 4