724 related articles for article (PubMed ID: 8116670)
1. 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]
2. Double trisomy (48,XXX, +18).
Tsukahara M; Fukuda M; Furukawa S; Kondoh O
Am J Med Genet; 1994 Aug; 52(2):244. PubMed ID: 7802021
[No Abstract] [Full Text] [Related]
3. Double trisomy 48,XXX,+ 18 in a newborn.
Rosenfeld W; Verma RS; Jhaveri RC; Salazar D; Dosik H
Am J Med Genet; 1981; 8(1):67-71. PubMed ID: 7246607
[TBL] [Abstract][Full Text] [Related]
4. [Trisomy 5p: a report of 2 cases].
Alvarez-Coca J; García-Alix A; Delicado A; González M; Escribá R; López Pajares I; Morena V; Peralta A
An Esp Pediatr; 1985 Mar; 22(4):288-92. PubMed ID: 4003955
[TBL] [Abstract][Full Text] [Related]
5. "Pure" partial trisomy 3p due to the malsegregation of a balanced maternal translocation t (X;3) (p22.3;p21).
de Almeida JC; Reis DF; Llerena JC; Pereira ET
Ann Genet; 1989; 32(3):181-3. PubMed ID: 2817779
[TBL] [Abstract][Full Text] [Related]
6. [Trisomy 5p due to paternal translocation (4;5) (q35;p12)].
Menéndez I; Casaña H
Bol Med Hosp Infant Mex; 1993 Mar; 50(3):194-6. PubMed ID: 8442884
[TBL] [Abstract][Full Text] [Related]
7. A case of 48, XXX, +18 double trisomy.
Imai I; Shimao S; Suzuki Y; Okada T
Acta Paediatr Jpn; 1987 Feb; 29(1):178-81. PubMed ID: 3144845
[No Abstract] [Full Text] [Related]
8. [Trisomy 18 or Edwards' syndrome. A report of 4 clinical cases].
Giaccardi A; Sardi R; Priora U; Vivalda M; Domeneghetti G; Girone P
Minerva Pediatr; 1991 Apr; 43(4):343-9. PubMed ID: 1870543
[TBL] [Abstract][Full Text] [Related]
9. Distal trisomy 14q due to tandem duplication (q24 leads to q32).
Orye E; Van Bever H; Desimpel H
Ann Genet; 1983; 26(4):238-9. PubMed ID: 6607705
[TBL] [Abstract][Full Text] [Related]
10. Secondary trisomy or mosaic "tetrasomy" 8p.
Robinow M; Haney N; Chen H; Sorauf T; Van Dyke DL; Babu VR; Powell S; Maliszewski W; Guerin S; Landers JW
Am J Med Genet; 1989 Mar; 32(3):320-4. PubMed ID: 2729351
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Branchial arch anomalies in trisomy 18.
Verloes A; Seret N; Bernier V; Gonzales M; Herens C; Koulischer L
Ann Genet; 1991; 34(1):22-4. PubMed ID: 1952786
[TBL] [Abstract][Full Text] [Related]
14. [A new case of trisomy 5p].
Antonenko VG; Levina LIa; Chudnova VI
Genetika; 1985 Dec; 21(12):2066-70. PubMed ID: 4085794
[TBL] [Abstract][Full Text] [Related]
15. A case of mosaic trisomy 14 due to an isochromosome, i(14q).
Ozawa N; Xu ZD; Soh K; Takabayashi T; Sato S; Yajima A; Suzuki M; Ikeuchi T; Tonomura A
Jinrui Idengaku Zasshi; 1984 Mar; 29(1):69-76. PubMed ID: 6748330
[No Abstract] [Full Text] [Related]
16. Trisomy 22: no longer an enigma.
Kukolich MK; Kulharya A; Jalal SM; Drummond-Borg M
Am J Med Genet; 1989 Dec; 34(4):541-4. PubMed ID: 2624265
[TBL] [Abstract][Full Text] [Related]
17. Clinical and postmortem findings of two cases with karyotype: 48, XXX, +18.
Sonoda T; Ohdo S; Madokoro H; Akimoto K; Ohba K
Acta Paediatr Jpn; 1987 Feb; 29(1):173-7. PubMed ID: 3144844
[No Abstract] [Full Text] [Related]
18. Multiple congenital anomalies associated with a 47,XXX chromosome constitution.
Hood OJ; Hartwell EA; Shattuck KE; Rosenberg HS
Am J Med Genet; 1990 May; 36(1):73-5. PubMed ID: 2333909
[TBL] [Abstract][Full Text] [Related]
19. Direct duplication of chromosome 1, dir dup(1)(p21.2----p32) in a Bedouin boy with multiple congenital anomalies.
Mohammed FM; Farag TI; Gunawardana SS; al-Digashim DD; al-Awadi SA; al-Othman SA; Sundareshan TS
Am J Med Genet; 1989 Mar; 32(3):353-5. PubMed ID: 2729356
[TBL] [Abstract][Full Text] [Related]
20. Trisomy 18 with unilateral atypical ectrodactyly.
Rogers RC
Am J Med Genet; 1994 Jan; 49(1):125-7. PubMed ID: 8172239
[No Abstract] [Full Text] [Related]
[Next] [New Search]