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Clinical genetics

Showing results (381-390 of 7,173) with videos related to

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Clinical Genetics|May 7, 2021
Spinocerebellar ataxia type 2 from an evolutionary perspective: Systematic review and meta-analysisLucas Schenatto Sena, Jordânia Dos Santos Pinheiro, Ali Hasan, et al.
Clinical Genetics|May 20, 2015
Exploration of the cognitive, adaptive and behavioral functioning of patients affected with Bardet-Biedl syndromeE N Kerr, A Bhan, E Héon
Clinical Genetics|June 18, 2015
Uptake of health monitoring and disease self-management in Australian adults with neurofibromatosis type 1: strategies to improve careH A Crawford, B Barton, M J Wilson, et al.
Clinical Genetics|June 18, 2015
Psychiatric and cognitive symptoms in Huntington's disease are modified by polymorphisms in catecholamine regulating enzyme genesT Vinther-Jensen, T T Nielsen, E Budtz-Jørgensen, et al.
Clinical Genetics|July 11, 1998
Clinical, biochemical and molecular findings in a two-generation Morquio A familyA Tylki-Szymańska, B Czartoryska, S Bunge, et al.
Clinical Genetics|July 11, 1998
Noonan syndrome associated with central giant cell granulomaB Uçar, A Okten, H Mocan, et al.
Clinical Genetics|April 24, 2020
ADAMTS19-associated heart valve defects: Novel genetic variants consolidating a recognizable cardiac phenotypeSalam Massadeh, Amal Alhashem, Ingrid M B H van de Laar, et al.
Clinical Genetics|June 13, 2020
Expanding the phenotypic spectrum consequent upon de novo WDR37 missense variantsEleanor Hay, Robert H Henderson, Sahar Mansour, et al.
Clinical Genetics|August 23, 2021
A novel POF1B variant in a Chinese patient is associated with premature ovarian failureZhuang-Zhuang Yuan, Chen-Yu Wang, Jie-Yuan Jin, et al.
Clinical Genetics|May 1, 2020
A novel TRAF3IP2 variant causing familial scarring alopecia with mixed features of discoid lupus erythematosus and folliculitis decalvansGeorges Nemer, Nehme El-Hachem, Edward Eid, et al.
Pageof 718

Showing results (381-390 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|May 7, 2021
Spinocerebellar ataxia type 2 from an evolutionary perspective: Systematic review and meta-analysisLucas Schenatto Sena, Jordânia Dos Santos Pinheiro, Ali Hasan, et al.
Clinical Genetics|May 20, 2015
Exploration of the cognitive, adaptive and behavioral functioning of patients affected with Bardet-Biedl syndromeE N Kerr, A Bhan, E Héon
Clinical Genetics|June 18, 2015
Uptake of health monitoring and disease self-management in Australian adults with neurofibromatosis type 1: strategies to improve careH A Crawford, B Barton, M J Wilson, et al.
Clinical Genetics|June 18, 2015
Psychiatric and cognitive symptoms in Huntington's disease are modified by polymorphisms in catecholamine regulating enzyme genesT Vinther-Jensen, T T Nielsen, E Budtz-Jørgensen, et al.
Clinical Genetics|July 11, 1998
Clinical, biochemical and molecular findings in a two-generation Morquio A familyA Tylki-Szymańska, B Czartoryska, S Bunge, et al.
Clinical Genetics|July 11, 1998
Noonan syndrome associated with central giant cell granulomaB Uçar, A Okten, H Mocan, et al.
Clinical Genetics|April 24, 2020
ADAMTS19-associated heart valve defects: Novel genetic variants consolidating a recognizable cardiac phenotypeSalam Massadeh, Amal Alhashem, Ingrid M B H van de Laar, et al.
Clinical Genetics|June 13, 2020
Expanding the phenotypic spectrum consequent upon de novo WDR37 missense variantsEleanor Hay, Robert H Henderson, Sahar Mansour, et al.
Clinical Genetics|August 23, 2021
A novel POF1B variant in a Chinese patient is associated with premature ovarian failureZhuang-Zhuang Yuan, Chen-Yu Wang, Jie-Yuan Jin, et al.
Clinical Genetics|May 1, 2020
A novel TRAF3IP2 variant causing familial scarring alopecia with mixed features of discoid lupus erythematosus and folliculitis decalvansGeorges Nemer, Nehme El-Hachem, Edward Eid, et al.
Pageof 718