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Clinical genetics

Showing results (581-590 of 7,173) with videos related to

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Clinical Genetics|October 1, 1976
A simple, rapid method for prenatal detection of defects in propionate metabolismG Morrow, B Revsin, C Mathews, et al.
Clinical Genetics|January 10, 2001
Ventricular septal defect associated with microdeletions of chromosome 22q11.2H Yamagishi, J Maeda, M Tokumura, et al.
Clinical Genetics|August 17, 2000
Atypical movement disorders in the early stages of Huntington's disease: clinical and genetic analysisF Squitieri, A Berardelli, E Nargi, et al.
Clinical Genetics|August 17, 2000
Cortical dysgenesis in 2 patients with chromosome 22q11 deletionL M Bird, P Scambler
Clinical Genetics|November 24, 1999
Detection of a novel germline mutation in the von Hippel-Lindau tumour-suppressor gene by fluorescence-labelled base excision sequence scanning (F-BESS)J Brieger, E J Weidt, K Gansen, et al.
Clinical Genetics|November 24, 1999
Fetal anticonvulsant syndrome and mutation in the maternal MTHFR geneJ C Dean, S J Moore, A Osborne, et al.
Clinical Genetics|October 12, 1999
Short rib-polydactyly syndrome: more evidence of a continuous spectrumK Sarafoglou, E F Funai, N Fefferman, et al.
Clinical Genetics|October 12, 1999
Aicardi-Goutières syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?S Fauré, I Bordelais, C Marquette, et al.
Clinical Genetics|June 14, 2000
Localization of an acromesomelic dysplasia on chromosome 9 by homozygosity mappingP Ianakiev, M W Kilpatrick, M J Daly, et al.
Clinical Genetics|June 14, 2000
Molecular analysis of Y chromosome long arm structural instability in patients with gonadal dysfunctionL Jakubowski, A Jeziorowska, M Constantinou, et al.
Pageof 718

Showing results (581-590 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|October 1, 1976
A simple, rapid method for prenatal detection of defects in propionate metabolismG Morrow, B Revsin, C Mathews, et al.
Clinical Genetics|January 10, 2001
Ventricular septal defect associated with microdeletions of chromosome 22q11.2H Yamagishi, J Maeda, M Tokumura, et al.
Clinical Genetics|August 17, 2000
Atypical movement disorders in the early stages of Huntington's disease: clinical and genetic analysisF Squitieri, A Berardelli, E Nargi, et al.
Clinical Genetics|August 17, 2000
Cortical dysgenesis in 2 patients with chromosome 22q11 deletionL M Bird, P Scambler
Clinical Genetics|November 24, 1999
Detection of a novel germline mutation in the von Hippel-Lindau tumour-suppressor gene by fluorescence-labelled base excision sequence scanning (F-BESS)J Brieger, E J Weidt, K Gansen, et al.
Clinical Genetics|November 24, 1999
Fetal anticonvulsant syndrome and mutation in the maternal MTHFR geneJ C Dean, S J Moore, A Osborne, et al.
Clinical Genetics|October 12, 1999
Short rib-polydactyly syndrome: more evidence of a continuous spectrumK Sarafoglou, E F Funai, N Fefferman, et al.
Clinical Genetics|October 12, 1999
Aicardi-Goutières syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?S Fauré, I Bordelais, C Marquette, et al.
Clinical Genetics|June 14, 2000
Localization of an acromesomelic dysplasia on chromosome 9 by homozygosity mappingP Ianakiev, M W Kilpatrick, M J Daly, et al.
Clinical Genetics|June 14, 2000
Molecular analysis of Y chromosome long arm structural instability in patients with gonadal dysfunctionL Jakubowski, A Jeziorowska, M Constantinou, et al.
Pageof 718