Partial deletion 10qter. a new case
Vanlieferinghen, P.; Dechelotte, P.; Charbonné, F.
Annales de Genetique 30(2): 118-121
1987
ISSN/ISBN: 0003-3995 PMID: 3314664 Document Number: 294593
A newborn with 10qter deletion is described and compared with the others previously reported cases. We confirm that the clinical features are not characteristic enough to delineate a syndrome in this chromosomal abnormality.
Document emailed within 1 workday
Related Documents
Lukusa, T.; Devriendt, K.; Fryns, J.P. 1999: A 3p deletion syndrome in a child with both del(3)(p25-->pter) and dup(17)(q23-->qter) Annales de Genetique 42(2): 91-94Vaillaud, J.C.; Martin, J.; Ayraud, N. 1970: A recent case of partial deletion of short arm of chromosome 18 Annales de Genetique 13(2): 120-122
Dallapiccola, B.; Marino, B.; Giannotti, A.; Valorani, G. 1989: Digeorge anomaly associated with partial deletion of chromosome 22. Report of a case with X/22 translocation and review of the literature Annales de Genetique 32(2): 92-96
Rosenmann, A.; Isacson, M.; Cohen, R.; Segal, M.; Cohen, M.M. 1978: Partial trisomy 18(q11 leads to qter) in an infant and aborted fetus resulting from a balanced paternal translocation t(13;18)(q32:q11) Annales de Genetique 21(1): 60-64
Hsu, H.L.; Hsiao, P.H.; Hou, J.W.; Tsai, W.Y.; Wang, T.R. 1997: Partial DiGeorge anomaly associated with 10p deletion Journal of the Formosan Medical Association 96(12): 996-999
Serville, F.; Allain, D.; Broustet, A.; Martin, C.; Gachet, M.; Babin, J.P.; Cenraud, J. 1976: Partial deletion of the short arm of the chromosome 9 Annales de Genetique 19(2): 143
De la Fuente, A.A.; Gerssen-Schoorl, K.B.; Breed, A.S. 1988: Partial duplication 14q/deletion 2q in two sibs due to t(2;14) (q37.1;q31.2) pat Annales de Genetique 31(4): 254-257
Saat, H.; Soysal, Y.; Kurtgoz, S.; Ergun, M.A.; Percin, E.F. 2015: A Patient with Partial Chromosome 12q Duplication and 10q Deletion Genetic Counseling 26(4): 401-407
Migliori, V.; Ferrari, F.; Giamagli, C.A.; DI Stefano, P.; Galanti, E.; Guastaferro, N. 1983: A case of 3q21-qter trisomy and 3p25-pter monosomy syndrome La Pediatria Medica e Chirurgica: Medical and Surgical Pediatrics 5(4): 237-239
Barletta, C.; Werner, B.; Ferrante, E.; Multari, G.; Tozzi, M.C.; Digilio, G.; Vignetti, P. 1985: Partial deletion of the long arm of chromosome 17 in acute promyelocitic leukemia Haematologica 70(2): 171-173
El-Bassyouni, H.T.; El-Gerzawy, A.M.S.; Mohamed, A.M.; Kamel, A.K.; Hussein, H.A.; Thomas, M.M.; El-Ruby, M. 2014: Terminal 2q deletion and partial trisomy chromosome 15q: a clinical and cytogenetic study Genetic Counseling 25(2): 151-158
Iannetti, P.; Spalice, A.; Mingarelli, R.; Raucci, U.; Novelli, A.; Dallapiccola, B. 1996: Myoclonic epilepsy, neuroblast migration disorders, and maternally derived partial duplication 14q/deletion 15q Annales de Genetique 39(1): 26-30
Hinton, R.B.; Deutsch, G.H.; Pearl, J.M.; Hobart, H.H.; Morris, C.A.; Benson, D.W. 2006: Bilateral semilunar valve disease in a child with partial deletion of the Williams-Beuren syndrome region is associated with elastin haploinsufficiency Journal of Heart Valve Disease 15(3): 352-355
Say, B.; Guzoglu, N.; Uras, N.; Candemir, Z.; Akin, I.; Dilmen, U. 2013: Partial trisomy 3p and partial monosomy 11q associated with double outlet right ventricle and septum pellucidum et vergae: a case report Genetic Counseling 24(4): 387-391
Petrishchev, V.N.; Kutueva, A.B.; Rychkov, I.G. 1993: Deletion-insertion polymorphism in the V-region of mitochondrial DNA in ten Mongoloid populations of Siberia, Frequency of deletion correlates with the geographic coordinates of the locality Genetika 29(7): 1196-1204
Alfi, O.; Donnell, G.N.; Crandall, B.F.; Derencsenyi, A.; Menon, R. 1973: Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome Annales de Genetique 16(1): 17-22
Richkind, K.E.; Lamb, A.; Lytle, C.; Velasco, J. 1996: A third case of apparent t(2;4)(p23;q25) represents ins(2;4) with deletion of 2p Leukemia 10(11): 1847
Karaman, A.; Aydin, H.; Geçkinli, B.; Göksu, K. 2015: The deletion 22q13 syndrome: a new case Genetic Counseling 26(1): 53-60
D'Oelsnitz, M.; Ayraud, N.; de Swarte, M.; Vaillant, J.M.; Darcourt, G. 1970: A case of deletion of short arm of chromosome 18 Pediatrie 25(2): 213-214
Mountz, J.D.; Mushinski, J.F.; Owens, J.D.; Finkelman, F.D. 1990: The in vivo generation of murine IgD-secreting cells is accompanied by deletion of the C mu gene and occasional deletion of the gene for the C delta 1 domain Journal of Immunology 145(5): 1583-1591