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Journal Abstract Search
98 related items for PubMed ID: 6971621
1. Partial trisomy 20. Delicado A, Lopez Pajares I, Vicente P, Gracia R. Ann Genet; 1981; 24(1):54-6. PubMed ID: 6971621 [Abstract] [Full Text] [Related]
2. [Syndrome of congenital malformations and dysmorphic features in a newborn with partial trisomy 16q due to maternal translocation t(9;16)(p24;q13)]. Luberda-Zapaśnik J, Midro AT, Szwałkiewicz-Warowicka E. Pediatr Pol; 1995 Sep; 70(9):769-73. PubMed ID: 8657511 [Abstract] [Full Text] [Related]
3. [Partial 11q trisomy due to missegregation of maternal t(11;22) (q23;q11.1) translocation (author's transl)]. Pangalos C, Couturier J, Bartsocas C, Theodorou S. Nouv Presse Med; 1980 Nov 01; 9(41):3065-7. PubMed ID: 7443445 [Abstract] [Full Text] [Related]
5. Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20. Okada M, Usami A, Okajima K, Yamada M, Yamaguchi Y, Umezaki I, Matsuda Y, Ohta H. Congenit Anom (Kyoto); 2005 Dec 01; 45(4):161-4. PubMed ID: 16359498 [Abstract] [Full Text] [Related]
6. Trisomy 3 (p23-pter) resulting from maternal translocation, t (3 ; 4)(p23 ; q35). Schinzel A, Hanson JW, Pagon RA, Hoehn H, Smith DW. Ann Genet; 1978 Sep 01; 21(3):168-71. PubMed ID: 315193 [Abstract] [Full Text] [Related]
7. Partial trisomy 13 with phenotype of Patau syndrome due to maternal reciprocal translocation t(6;13) (q25;q13). Petit P, Fryns JP, van den Berghe H. Ann Genet; 1980 Sep 01; 23(1):57-9. PubMed ID: 6965845 [No Abstract] [Full Text] [Related]
8. [Marker chromosomes as a product of familial translocation (11;22) identified with molecular cytogenetic methods]. Stankiewicz P, Korniszewski L, Bocian E, Stańczak H. Pediatr Pol; 1996 Mar 01; 71(3):241-5. PubMed ID: 8966096 [Abstract] [Full Text] [Related]
9. Mild dysmorphic signs in two male sibs with partial trisomy 2q32.1-->q35 due to maternal ins(14;2) translocation. Lukusa T, Devriendt K, Jaeken J, Fryns JP. Clin Dysmorphol; 1999 Jan 01; 8(1):47-51. PubMed ID: 10327251 [Abstract] [Full Text] [Related]
10. Trisomy 16p in a liveborn offspring due to maternal translocation t(16;21)(q11;p11) and review of the literature. Léonard C, Huret JL, Imbert MC, Lebouc Y, Selva J, Boulley AM. Am J Med Genet; 1992 Jun 01; 43(3):621-5. PubMed ID: 1605261 [Abstract] [Full Text] [Related]
11. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development. Ausems MG, Van Spijker HG, Dijkhuis HJ, Swanenburg De Veye HF, Bijlsma JB. Genet Couns; 1996 Jun 01; 7(1):61-5. PubMed ID: 8652090 [Abstract] [Full Text] [Related]
12. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation. Tüysüz B, Hacihanefioglu S, Silahtaroglu A, Yilmaz S, Deviren A, Cenani A. Genet Couns; 2000 Jun 01; 11(4):355-61. PubMed ID: 11140413 [Abstract] [Full Text] [Related]
14. Partial trisomy of the distal part of 10q: a report of two Egyptian cases. Aglan MS, Kamel AK, Helmy NA. Genet Couns; 2008 Jun 01; 19(2):199-209. PubMed ID: 18618995 [Abstract] [Full Text] [Related]
15. An unusual clinical characterization of a male with distal partial trisomy 1q42.1 and monosomy 4q35.1 and review of the literature. Wang CB, Lin SP, Chen CP, Chen YJ, Lee CC. Genet Couns; 2006 Jun 01; 17(4):435-40. PubMed ID: 17375530 [Abstract] [Full Text] [Related]
16. [Trisomy 5p due to paternal translocation (4;5) (q35;p12)]. Menéndez I, Casaña H. Bol Med Hosp Infant Mex; 1993 Mar 01; 50(3):194-6. PubMed ID: 8442884 [Abstract] [Full Text] [Related]