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E Orye

Showing results (1-10 of 21) with videos related to

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Humangenetik|August 25, 1975
Short arm deletion of chromosome 12: report of two new casesE Orye, M Craen
Annales De Genetique|January 1, 1984
Trisomy 3p syndrome. Report of a new case, due to a chromosomal insertionE Orye, G Laureys
Clinical Genetics|March 1, 1976
A new chromosome deletion syndrome. Report of a patient with a 46,XY,8p- chromosome constitutionE Orye, M Craen
Acta Geneticae Medicae Et Gemellologiae|January 1, 1975
Unexpected findings with the new chromosome banding techniques in a patient formerly diagnosed as having G-deletion syndrome IIE Orye, M Craen
Annales De Genetique|January 1, 1985
De novo distal trisomy 17qE Orye, H van Bever
Annales De Genetique|January 1, 1985
Mosaic and non-mosaic trisomy 15q2E Orye, G Laureys, H Verhaaren
Histochemistry|January 1, 1984
Beta-glucuronidase activity in human T and B lymphocytes and the Tmu and T gamma subpopulationsE Orye, J Plum, M De Smedt
Annales De Genetique|January 1, 1983
Distal trisomy 14q due to tandem duplication (q24 leads to q32)E Orye, H Van Bever, H Desimpel
Journal of Medical Genetics|October 1, 1983
Complete trisomy 5p owing to de novo translocation t(5;22)(q11;p11) with isochromosome 5p associated with a familial pericentric inversion of chromosome 2, inv 2(p21q11)E Orye, Y Benoit, B van Mele
Humangenetik|May 26, 1975
A 46,XX,10Q+ chromosome constitution in a girl. Partial long arm duplication or insertional translocation?E Orye, H Verhaaren, K Samuël, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Humangenetik|August 25, 1975
Short arm deletion of chromosome 12: report of two new casesE Orye, M Craen
Annales De Genetique|January 1, 1984
Trisomy 3p syndrome. Report of a new case, due to a chromosomal insertionE Orye, G Laureys
Clinical Genetics|March 1, 1976
A new chromosome deletion syndrome. Report of a patient with a 46,XY,8p- chromosome constitutionE Orye, M Craen
Acta Geneticae Medicae Et Gemellologiae|January 1, 1975
Unexpected findings with the new chromosome banding techniques in a patient formerly diagnosed as having G-deletion syndrome IIE Orye, M Craen
Annales De Genetique|January 1, 1985
De novo distal trisomy 17qE Orye, H van Bever
Annales De Genetique|January 1, 1985
Mosaic and non-mosaic trisomy 15q2E Orye, G Laureys, H Verhaaren
Histochemistry|January 1, 1984
Beta-glucuronidase activity in human T and B lymphocytes and the Tmu and T gamma subpopulationsE Orye, J Plum, M De Smedt
Annales De Genetique|January 1, 1983
Distal trisomy 14q due to tandem duplication (q24 leads to q32)E Orye, H Van Bever, H Desimpel
Journal of Medical Genetics|October 1, 1983
Complete trisomy 5p owing to de novo translocation t(5;22)(q11;p11) with isochromosome 5p associated with a familial pericentric inversion of chromosome 2, inv 2(p21q11)E Orye, Y Benoit, B van Mele
Humangenetik|May 26, 1975
A 46,XX,10Q+ chromosome constitution in a girl. Partial long arm duplication or insertional translocation?E Orye, H Verhaaren, K Samuël, et al.
Pageof 3