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2. [Partial trisomy 9q: description of a new case]. Pirovano S; Sangermani R; Rossi A; Tornaghi R; Magnani I; Fuhrman Conti AM; Garrone A; Vaccari R Pediatr Med Chir; 1983; 5(1-2):111-3. PubMed ID: 6634434 [TBL] [Abstract][Full Text] [Related]
3. [Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation]. Fioretti G; Pagano L; Renda S; Festa B; Rinaldi A; Celona A; Casullo C; Stabile M; Cavaliere ML; Ventruto V Minerva Pediatr; 1980 Jun; 32(12):807-14. PubMed ID: 7464734 [No Abstract] [Full Text] [Related]
4. [12 p trisomy. A new case (author's transl)]. Kubryk N; Prieur M; Borde M Ann Pediatr (Paris); 1980 Dec; 27(10):695-9. PubMed ID: 7212558 [No Abstract] [Full Text] [Related]
5. [Trisomy 8 as a defined clinical entity]. Zergollern L; Valjak B; Muzinić D Acta Med Iugosl; 1975; 29(5):409-19. PubMed ID: 1199796 [No Abstract] [Full Text] [Related]
6. [Trisomy 10 p. Apropos of a case caused by a maternal translocation]. Stoll C; Willard D Pediatrie; 1980; 35(3):251-5. PubMed ID: 7393692 [No Abstract] [Full Text] [Related]
7. Trisomy of the short arm of chromosome number 9: a clinical entity. Fryns JP; van den Berghe H Acta Paediatr Belg; 1980; Suppl 13():97-104. PubMed ID: 7415833 [No Abstract] [Full Text] [Related]
8. [Trisomy 10p as a result of familial 10/22 translocation]. Zergollern L; Begovic D; Muzinić D Acta Med Iugosl; 1980; 34(2):113-22. PubMed ID: 7405617 [No Abstract] [Full Text] [Related]
9. [Prenatal diagnosis of a de novo trisomy case 9q-47,XX,+9 del(q33----qter)]. Cordier MP; Coicaud C; Thoulon JM; Robert JM; Germain D J Genet Hum; 1984 Dec; 32(5):351-61. PubMed ID: 6527131 [TBL] [Abstract][Full Text] [Related]
10. Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literature. Taysi K; Chao WT; Monaghan N; Monaco MP Ann Genet; 1983; 26(4):243-6. PubMed ID: 6364954 [TBL] [Abstract][Full Text] [Related]
11. [Enzyme activity of red blood cells in a child with chromosome 8 trisomy]. Rogóyski A; Jabłońska-Skwiecińska E; Tronowska TD Pediatr Pol; 1982; 57(10):799-801. PubMed ID: 7182765 [No Abstract] [Full Text] [Related]
12. [Rethoré syndrome (9p trisomy) with unusual karyotype: 46,XX,-9, + der 9p, t(9;9)mat]. Di Cesare D; Paludetto R; Casullo C; Pagano L; Stabile M; Sicolo A; Ventruto V Minerva Pediatr; 1980 Dec; 32(23):1349-52. PubMed ID: 7219376 [No Abstract] [Full Text] [Related]
13. [Partial trisomy (10pter leads to 10q21) and partial monosomy (21pter leads to 21q21) due to a reciprocal balanced familial translocation (10;21)(q21;q21) (author's transl)]. Obry E; Piussan C; Risbourg B; Dutrillaux B Ann Genet; 1980; 23(4):216-20. PubMed ID: 6971599 [TBL] [Abstract][Full Text] [Related]
18. Partial trisomy 8 mosaicism with 46,XX/46,XX-8,+dic(8). Ray M; Hunter AG Ann Genet; 1980; 23(2):100-2. PubMed ID: 6967279 [TBL] [Abstract][Full Text] [Related]
19. Partial trisomy 12p. A newborn child with karyotype 46,XY,der(11), t(11; 12) (q25; p11) mat. Case report and review. Ottolina de Bracamonte N; Velazco JQ; Hammond Figueroa FG Acta Cient Venez; 1982; 33(4):342-7. PubMed ID: 7186725 [No Abstract] [Full Text] [Related]
20. [9p trisomy syndrome. Two new cases (author's transl)]. Martín Sánchez A; Delicado A; Izquierdo M; Oliver A; López Pajares I; Gracia R; Peralta A An Esp Pediatr; 1981 May; 14(5):344-51. PubMed ID: 7294523 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]