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2. Trisomy 6q25 to 6qter in a severely retarded 7-year-old boy with turricephaly, bow-shaped mouth, hypogenitalism and club feet. Schmid W; D'Apuzzo V; Rossi E Hum Genet; 1979 Feb; 46(3):279-84. PubMed ID: 437771 [TBL] [Abstract][Full Text] [Related]
3. Duplication 6q24 leads to 6qter in an infant from a balanced paternal translocation. Chase TR; Jalal SM; Martsolf JT; Wasdahl WA Am J Med Genet; 1983 Feb; 14(2):347-51. PubMed ID: 6837629 [TBL] [Abstract][Full Text] [Related]
4. Trisomy 6q25 leads to 6qter in two sisters resulting from maternal 6;11 translocation. Clark CE; Cowell HR; Telfer MA; Casey PA Am J Med Genet; 1980; 5(2):171-8. PubMed ID: 7395910 [TBL] [Abstract][Full Text] [Related]
5. Partial trisomy 12q24.31----qter. Tajara EH; Varella-Garcia M; Gusson AC J Med Genet; 1985 Feb; 22(1):73-6. PubMed ID: 3981585 [TBL] [Abstract][Full Text] [Related]
6. Duplication 6q syndrome. Tipton RE; Berns JS; Johnson WE; Wilroy RS; Summitt RL Am J Med Genet; 1979; 3(4):325-30. PubMed ID: 474632 [TBL] [Abstract][Full Text] [Related]
7. Trisomy 12p syndrome. Evaluation of a family with a t(12;21) (p12.1;p11) translocation with unbalanced offspring. Hansteen IL; Schirmer L; Hestetun S Clin Genet; 1978 Apr; 13(4):339-49. PubMed ID: 148983 [TBL] [Abstract][Full Text] [Related]
8. Partial trisomy 8q in half-sisters with distinct dysmorphic patterns not similar to the trisomy 8 mosaicism syndrome. Schinzel A Hum Genet; 1977 Jun; 37(1):17-26. PubMed ID: 881192 [TBL] [Abstract][Full Text] [Related]
9. Trisomy 9 mosaicism in two girls with multiple congenital malformations and mental retardation. Stoll C; Chognot D; Halb A; Luckel JC J Med Genet; 1993 May; 30(5):433-5. PubMed ID: 8320712 [TBL] [Abstract][Full Text] [Related]
10. Partial trisomy 10q: a recognizable syndrome. Klep-de Pater JM; Bijlsma JB; de France HF; Leschot NJ; Duijndam-van den Berge M; van Hemel JO Hum Genet; 1979 Jan; 46(1):29-40. PubMed ID: 429004 [TBL] [Abstract][Full Text] [Related]
11. Pure partial trisomy for long arm of chromosome 9. Faed M; Robertson J; Brown S; Smail PJ; Muckhart RD J Med Genet; 1976 Jun; 13(3):239-42. PubMed ID: 933125 [TBL] [Abstract][Full Text] [Related]
12. Tandem duplication (1) (q11----q22) in a male infant with multiple congenital malformations. Mertens F; Johansson B; Forslund M; Olsson M; Kristoffersson U Clin Genet; 1987 Jul; 32(1):46-8. PubMed ID: 3621653 [TBL] [Abstract][Full Text] [Related]
13. New autosomal syndromes: trisomies 4p and 9p. Dallapiccola B; Mastroiacovo P; Segni G Acta Genet Med Gemellol (Roma); 1977; 26(3-4):267-73. PubMed ID: 613692 [No Abstract] [Full Text] [Related]
14. Trisomy 10p due to a de novo t(10p;13p). Aller V; Abrisqueta JA; Pérez-Castillo A; del Mazo J; Martín-Lucas MA; de Torres ML Hum Genet; 1979 Jan; 46(2):129-34. PubMed ID: 422195 [TBL] [Abstract][Full Text] [Related]
15. 'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations. Brimblecombe FS; Lewis FJ; Vowles M J Med Genet; 1977 Aug; 14(4):271-4. PubMed ID: 926139 [TBL] [Abstract][Full Text] [Related]
16. Trisomy 9 mosaicism with multiple congenital anomalies. Haslam RH; Broske SP; Moore CM; Thomas GH; Neill CA J Med Genet; 1973 Jun; 10(2):180-4. PubMed ID: 4714587 [TBL] [Abstract][Full Text] [Related]
17. Trisomy 4p in four relatives: variability and lack of distinctive features in phenotypic expression. Reynolds JF; Shires MA; Wyandt HE; Kelly TE Clin Genet; 1983 Nov; 24(5):365-74. PubMed ID: 6418421 [TBL] [Abstract][Full Text] [Related]
18. Partial trisomy of the short arm of chromosome 7 due to a familial translocation rcp(7;14)(p11;p11). Carnevale A; Frías S; del Castillo V Clin Genet; 1978 Oct; 14(4):202-6. PubMed ID: 699358 [TBL] [Abstract][Full Text] [Related]