224 related articles for article (PubMed ID: 7122200)
1. The trisomy 9-syndrome.
Carpenter BF; Tomkins DJ
Perspect Pediatr Pathol; 1982; 7():109-20. PubMed ID: 7122200
[No Abstract] [Full Text] [Related]
2. The distal 9p trisomy syndrome: a major clinical-cytogenetic entity.
Centerwall WR
Birth Defects Orig Artic Ser; 1977; 13(3D):165-77. PubMed ID: 922135
[No Abstract] [Full Text] [Related]
3. Trisomy 18-Edwards syndrome: a report of three patients.
Ejiwumni AB; Msamati BC
Cent Afr J Med; 1993 May; 39(5):105-9. PubMed ID: 8131193
[No Abstract] [Full Text] [Related]
4. [Partial C trisomy through translocation t(Cp-;Gp-)].
Deminatti M; Maillard E; Gosselin B; Peltier JM; Bulteel MF; Dupuis C
Ann Genet; 1969 Mar; 12(1):36-45. PubMed ID: 5306710
[No Abstract] [Full Text] [Related]
5. [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]
6. [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]
7. [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]
8. Partial trisomy 10q in three unrelated patients.
Taysi K; Yang V; Monaghan N; Beraha N
Ann Genet; 1983; 26(2):79-85. PubMed ID: 6604490
[TBL] [Abstract][Full Text] [Related]
9. [Apropos of trisomy 18 - a study of 4 observations].
Gilgenkrantz S; Sapelier J; Thiriet M; Kahn C; Pierson M
Ann Genet; 1967 Mar; 10(1):32-8. PubMed ID: 5300124
[No Abstract] [Full Text] [Related]
10. [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]
11. Developmental and other pathologic changes in syndromes caused by chromosome abnormalities.
Gilbert EF; Opitz JM
Perspect Pediatr Pathol; 1982; 7():1-63. PubMed ID: 6214761
[No Abstract] [Full Text] [Related]
12. The trisomy 18 syndrome.
Zizka J; Dvorăcková I
Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove; 1967; 10(1):11-9. PubMed ID: 5239107
[No Abstract] [Full Text] [Related]
13. Partial trisomy 9q-in a polymalformed new-born infant. Karyotype: 47,XX, + del (9) (q33).
Fryns JP; Smeets E; Eggermont E; Delire C; Van den Berghe H
Acta Paediatr Belg; 1978; 31(4):237-40. PubMed ID: 742362
[No Abstract] [Full Text] [Related]
14. 13-15 (D1) trisomy syndrome. (With special emphasis on pathological findings).
Tun cbilek E; Balci S; Say B; Tinaztepe K
Turk J Pediatr; 1971 Jul; 13(3):112-24. PubMed ID: 5150867
[No Abstract] [Full Text] [Related]
15. Chromosome study of the family with a daughter showing 9p+ syndrome.
Santadusit A; Wangpreedalertkul W; Anusri Y; Meevatee U
J Med Assoc Thai; 1981 Sep; 64(9):480-4. PubMed ID: 7299300
[No Abstract] [Full Text] [Related]
16. 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]
17. An infant with double trisomy (48,XXX, + 18).
Jaruratanasirikul S; Jinorose U
Am J Med Genet; 1994 Jan; 49(2):207-10. PubMed ID: 8116670
[TBL] [Abstract][Full Text] [Related]
18. [Trisomy syndrome of the end section of the long arm of chromosome 4].
Stoll C; Roth MP; Dott B; Lutz P
Ann Pediatr (Paris); 1985 Jun; 32(6):527-30. PubMed ID: 4026150
[No Abstract] [Full Text] [Related]
19. Proximal 14 trisomy 46,XX, -22 +der(14)t(14;22) (q21;q11)mat.
Fried K; Goldberg MD; Rosenblatt M
Teratology; 1980 Jun; 21(3):309-12. PubMed ID: 7455919
[No Abstract] [Full Text] [Related]
20. [2 familial translocations occurring together in each of 2 sisters, one balanced, the other partial trisomic 10q].
de Grouchy J; Finaz C; Roubin M; Roy J
Ann Genet; 1972 Jun; 15(2):85-92. PubMed ID: 4537727
[No Abstract] [Full Text] [Related]
[Next] [New Search]
