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Humangenetik
|
August 25, 1975
Short arm deletion of chromosome 12: report of two new cases
E Orye, M Craen
Annales De Genetique
|
January 1, 1984
Trisomy 3p syndrome. Report of a new case, due to a chromosomal insertion
E Orye, G Laureys
Clinical Genetics
|
March 1, 1976
A new chromosome deletion syndrome. Report of a patient with a 46,XY,8p- chromosome constitution
E 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 II
E Orye, M Craen
Annales De Genetique
|
January 1, 1985
De novo distal trisomy 17q
E Orye, H van Bever
Annales De Genetique
|
January 1, 1985
Mosaic and non-mosaic trisomy 15q2
E Orye, G Laureys, H Verhaaren
Histochemistry
|
January 1, 1984
Beta-glucuronidase activity in human T and B lymphocytes and the Tmu and T gamma subpopulations
E 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.
Page
of 3
Search research articles
Search
Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
Humangenetik
|
August 25, 1975
Short arm deletion of chromosome 12: report of two new cases
E Orye, M Craen
Annales De Genetique
|
January 1, 1984
Trisomy 3p syndrome. Report of a new case, due to a chromosomal insertion
E Orye, G Laureys
Clinical Genetics
|
March 1, 1976
A new chromosome deletion syndrome. Report of a patient with a 46,XY,8p- chromosome constitution
E 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 II
E Orye, M Craen
Annales De Genetique
|
January 1, 1985
De novo distal trisomy 17q
E Orye, H van Bever
Annales De Genetique
|
January 1, 1985
Mosaic and non-mosaic trisomy 15q2
E Orye, G Laureys, H Verhaaren
Histochemistry
|
January 1, 1984
Beta-glucuronidase activity in human T and B lymphocytes and the Tmu and T gamma subpopulations
E 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.
Page
of 3