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22. A familial 10/13 translocation: partial trisomy C in an infant associated with familial 10/13 translocation. Mulcahy MT; Jenkyn J; Masters PL Clin Genet; 1974; 6(5):335-40. PubMed ID: 4434650 [No Abstract] [Full Text] [Related]
23. Cri-du-chat syndrome combined with partial C-group trisomy. Mann J; Rafferty JH J Med Genet; 1972 Sep; 9(3):289-92. PubMed ID: 5079100 [No Abstract] [Full Text] [Related]
24. Partial trisomy of chromosome 11: a case report. Falk RE; Carrel RE; Valente M; Crandall BF; Sparkes RS Am J Ment Defic; 1973 Jan; 77(4):383-8. PubMed ID: 4706396 [No Abstract] [Full Text] [Related]
25. A case of partial trisomy 8p resulting from a maternal balanced translocation. Clark CE; Telfer MA; Cowell HR Am J Med Genet; 1980; 7(1):21-5. PubMed ID: 7211950 [No Abstract] [Full Text] [Related]
26. 11q aneuploidy: partial monosomy and trisomy in the children of a mother with a t(3;11)(p27;q23) translocation. Ridler MA; McKeown JA Hum Genet; 1979 Nov; 52(1):101-6. PubMed ID: 527970 [TBL] [Abstract][Full Text] [Related]
27. Partial trisomy for 7p due to maternal balanced translocation. Ohdo S; Suzumori K; Madokoro H; Sonoda T; Hayakawa K Jinrui Idengaku Zasshi; 1983 Dec; 28(4):297-300. PubMed ID: 6678317 [No Abstract] [Full Text] [Related]
28. [Increase of the LDH-B activity in a boy with 12p trisomy by malsegregation of a maternal translocation t(12;14) (q12;p11)]. Rethoré MO; Kaplan JC; Junien C; Cruveiller J; Dutrillaux B; Aurias A; Carpentier S; Lafourcade J; Lejeune Ann Genet; 1975 Jun; 18(2):81-7. PubMed ID: 1081369 [TBL] [Abstract][Full Text] [Related]
29. [Trisomy 9p due to t(9p 14q) de novo]. Canki N; Rethoré MO; Ferrand J; Lejeune J Lijec Vjesn; 1975 Feb; 97(2):103-5. PubMed ID: 1160475 [No Abstract] [Full Text] [Related]
30. Familial inversion translocation (8;13) with partial trisomy 13 in several family members. Pilgaard B; Jørgensen E; Knudsen VS; Mortensen E; Mikkelsen M Eur J Pediatr; 1983 Apr; 140(2):105-8. PubMed ID: 6884384 [TBL] [Abstract][Full Text] [Related]
31. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study. Jacobsen P; Hauge M; Henningsen K; Hobolth N; Mikkelsen M; Philip J Hum Hered; 1973; 23(6):568-85. PubMed ID: 4134631 [No Abstract] [Full Text] [Related]
33. Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+). Tal'vik TA; Mikel'saar AV; Mikel'saar RV Sov Genet; 1974 Jun; 8(5):651-7. PubMed ID: 4413436 [No Abstract] [Full Text] [Related]
34. Partial trisomy 10q occurring in a family with a reciprocal translocation t(10;18)(q25;q23). Kroyer S; Niebuhr E Ann Genet; 1975 Mar; 18(1):50-5. PubMed ID: 50043 [TBL] [Abstract][Full Text] [Related]
35. C autosomal trisomy with mosaicism: a new syndrome? van Eys J; Nance WE; Engel E Pediatrics; 1970 Apr; 45(4):665-71. PubMed ID: 5467317 [No Abstract] [Full Text] [Related]
36. Partial trisomy 18 in a family with a translocation (18;21)(q21;q22). Niazi M; Coleman DV; Saldaña-Garcia P J Med Genet; 1978 Apr; 15(2):148-51. PubMed ID: 641950 [TBL] [Abstract][Full Text] [Related]