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Annales De Genetique|January 1, 1985
[Reciprocal syndromes caused by deficiency duplication resulting from maternal t(10;18)(p12;q22) translocation]M O Rethoré, M Prieur, M C de Blois, et al.Annales De Genetique|January 1, 1985
[Trisomy 20p derived from a maternal pericentric inversion and brachymesophalangy of the index finger]J Lucas, F Le Mée, B Le Marec, et al.Annales De Genetique|January 1, 1985
A familial paracentric inv(1)(q42q44) resulting in a child with a del(1)(q42) karyotypeM Speevak, A G Hunter, H Hughes, et al.Annales De Genetique|January 1, 1985
46,XX,-12,+der(12),rcp(3;12)(p25.1;p13.31)pat karyotype in a girl. Probable subregional assignment of glyceraldehyde-3-phosphate dehydrogenase locus to 12p13.1----p13.31 by exclusion mappingF Rivas, G Vaca, G Zúñiga, et al.Annales De Genetique|January 1, 1985
Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segmentD García-Cruz, L García-Esquivel, H Rivera, et al.Annales De Genetique|January 1, 1985
Consistent deficiencies of chromosome 18 and of the short arm of chromosome 17 in eleven cases of human large bowel cancer: a possible recessive determinismM Muleris, R J Salmon, B Zafrani, et al.Annales De Genetique|January 1, 1985
Translocation (X;13)(p11.21;q12.3) in a girl with incontinentia pigmenti and bilateral retinoblastomaT Kajii, M Tsukahara, Y Fukushima, et al.Annales De Genetique|January 1, 1985
The critical segment for the Langer-Giedion syndrome: 8q24.11----q24.12P Bowen, B Biederman, J J HooAnnales De Genetique|January 1, 1985
De novo interstitial deletion of the long arm of chromosome 7:46,XY,del(7)(q23;q32)B Martin-Pont, C Pilczer, M Dandine, et al.Pageof 129