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Clinical genetics

Showing results (231-240 of 7,173) with videos related to

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Clinical Genetics|June 6, 2003
Intact fetal cell isolation from maternal blood: improved isolation using a simple whole blood progenitor cell enrichment approach (RosetteSep)F Z Bischoff, D A Marquéz-Do, D I Martinez, et al.
Clinical Genetics|June 6, 2003
A novel dominant missense mutation--D179N--in the GJB2 gene (Connexin 26) associated with non-syndromic hearing lossP Primignani, P Castorina, F Sironi, et al.
Clinical Genetics|June 6, 2003
A novel syndrome of combined immunodeficiency, autoimmunity and spondylometaphyseal dysplasiaC M Roifman, I Melamed
Clinical Genetics|November 15, 2002
An unstable dicentric Robertsonian translocation in a markedly discordant twinR V Lebo, H E Wyandt, P E Warburton, et al.
Clinical Genetics|November 15, 2002
Ring syndrome caused by ring chromosome 7 without loss of subtelomeric sequencesJ R Vermeesch, E Baten, J-P Fryns, et al.
Clinical Genetics|October 10, 2002
Hair as a diagnostic tool in dysmorphologyM Silengo, M Valenzise, L Sorasio, et al.
Clinical Genetics|October 10, 2002
Acute intermittent porphyria in Sweden. Molecular, functional and clinical consequences of some new mutations found in the porphobilinogen deaminase geneY Floderus, P M Shoolingin-Jordan, P Harper
Clinical Genetics|November 15, 2002
Sleep disturbance in mucopolysaccharidosis type III (Sanfilippo syndrome): a survey of managing cliniciansJ Fraser, J E Wraith, M B Delatycki
Clinical Genetics|December 18, 2002
X-linked mental retardation: vanishing boundaries between non-specific (MRX) and syndromic (MRXS) formsS G M Frints, G Froyen, P Marynen, et al.
Clinical Genetics|January 1, 1976
A dermatoglyphic study of 219 Italian schizophrenic malesD Kemali, N Polani, P E Polani, et al.
Pageof 718

Showing results (231-240 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|June 6, 2003
Intact fetal cell isolation from maternal blood: improved isolation using a simple whole blood progenitor cell enrichment approach (RosetteSep)F Z Bischoff, D A Marquéz-Do, D I Martinez, et al.
Clinical Genetics|June 6, 2003
A novel dominant missense mutation--D179N--in the GJB2 gene (Connexin 26) associated with non-syndromic hearing lossP Primignani, P Castorina, F Sironi, et al.
Clinical Genetics|June 6, 2003
A novel syndrome of combined immunodeficiency, autoimmunity and spondylometaphyseal dysplasiaC M Roifman, I Melamed
Clinical Genetics|November 15, 2002
An unstable dicentric Robertsonian translocation in a markedly discordant twinR V Lebo, H E Wyandt, P E Warburton, et al.
Clinical Genetics|November 15, 2002
Ring syndrome caused by ring chromosome 7 without loss of subtelomeric sequencesJ R Vermeesch, E Baten, J-P Fryns, et al.
Clinical Genetics|October 10, 2002
Hair as a diagnostic tool in dysmorphologyM Silengo, M Valenzise, L Sorasio, et al.
Clinical Genetics|October 10, 2002
Acute intermittent porphyria in Sweden. Molecular, functional and clinical consequences of some new mutations found in the porphobilinogen deaminase geneY Floderus, P M Shoolingin-Jordan, P Harper
Clinical Genetics|November 15, 2002
Sleep disturbance in mucopolysaccharidosis type III (Sanfilippo syndrome): a survey of managing cliniciansJ Fraser, J E Wraith, M B Delatycki
Clinical Genetics|December 18, 2002
X-linked mental retardation: vanishing boundaries between non-specific (MRX) and syndromic (MRXS) formsS G M Frints, G Froyen, P Marynen, et al.
Clinical Genetics|January 1, 1976
A dermatoglyphic study of 219 Italian schizophrenic malesD Kemali, N Polani, P E Polani, et al.
Pageof 718