These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
119 related articles for article (PubMed ID: 3411398)
1. Confirmation of autosomal dominant transmission of the DiGeorge malformation complex. Keppen LD; Fasules JW; Burks AW; Gollin SM; Sawyer JR; Miller CH J Pediatr; 1988 Sep; 113(3):506-8. PubMed ID: 3411398 [No Abstract] [Full Text] [Related]
2. Interstitial deletion of chromosome 22 in a patient with the DiGeorge malformation sequence. Mascarello JT; Bastian JF; Jones MC Am J Med Genet; 1989 Jan; 32(1):112-4. PubMed ID: 2705472 [TBL] [Abstract][Full Text] [Related]
3. Partial monosomy 22 as result of an X/22 translocation in a newborn with DiGeorge syndrome. Schwanitz G; Zerres K Ann Genet; 1987; 30(2):80-4. PubMed ID: 3314667 [TBL] [Abstract][Full Text] [Related]
4. [Monosomy 22pter-22q11.2 with monosomy 10q26.2-10qter without Di George syndrome]. Arslanian A; Veneziano G; Grasso M; Brugo A; Bertamino F Pathologica; 1985; 77(1052):767-70. PubMed ID: 3842998 [No Abstract] [Full Text] [Related]
5. Digeorge anomaly associated with partial deletion of chromosome 22. Report of a case with X/22 translocation and review of the literature. Dallapiccola B; Marino B; Giannotti A; Valorani G Ann Genet; 1989; 32(2):92-6. PubMed ID: 2667458 [TBL] [Abstract][Full Text] [Related]
6. A case of incomplete DiGeorge syndrome associated with partial monosomy 22q11.1 due to maternal 14;22 translocation. Nukina S; Nishimura Y; Kinugasa A; Sawada T; Hamaoka K; Inazawa J; Tsuda S; Abe T Jinrui Idengaku Zasshi; 1989 Sep; 34(3):235-41. PubMed ID: 2634137 [TBL] [Abstract][Full Text] [Related]
7. The association of the DiGeorge anomalad with partial monosomy of chromosome 22. Kelley RI; Zackai EH; Emanuel BS; Kistenmacher M; Greenberg F; Punnett HH J Pediatr; 1982 Aug; 101(2):197-200. PubMed ID: 7097410 [TBL] [Abstract][Full Text] [Related]
8. A deletion in chromosome 22 can cause DiGeorge syndrome. de la Chapelle A; Herva R; Koivisto M; Aula P Hum Genet; 1981; 57(3):253-6. PubMed ID: 7250965 [TBL] [Abstract][Full Text] [Related]
10. Features of di George syndrome in a child with 45,XX,-3,-22,+der(3),t(3;22)(p25;q11). Faed MJ; Robertson J; Beck JS; Cater JI; Bose B; Madlom MM J Med Genet; 1987 Apr; 24(4):225-7. PubMed ID: 3585938 [TBL] [Abstract][Full Text] [Related]
11. T cell immunodeficiency in a patient with 10p deletion syndrome. Monaco G; Ciccimarra F; Pignata C; Garofalo S J Pediatr; 1989 Aug; 115(2):330. PubMed ID: 2754563 [No Abstract] [Full Text] [Related]
12. DiGeorge syndrome in a child with partial monosomy of chromosome 22. Annerén G; Gustafsson J; Sunnegårdh J Ups J Med Sci; 1989; 94(1):47-53. PubMed ID: 2711536 [TBL] [Abstract][Full Text] [Related]
13. Localization of 27 DNA markers to the region of human chromosome 22q11-pter deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndrome. Carey AH; Roach S; Williamson R; Dumanski JP; Nordenskjold M; Collins VP; Rouleau G; Blin N; Jalbert P; Scambler PJ Genomics; 1990 Jul; 7(3):299-306. PubMed ID: 2365351 [TBL] [Abstract][Full Text] [Related]
14. Cytogenetic findings in a prospective series of patients with DiGeorge anomaly. Greenberg F; Elder FF; Haffner P; Northrup H; Ledbetter DH Am J Hum Genet; 1988 Nov; 43(5):605-11. PubMed ID: 3189331 [TBL] [Abstract][Full Text] [Related]
15. Thymus deficiency in an infant with a chromosome t(18;22)(q12.2;p11.2)pat rearrangement. Bowen P; Pabst H; Berry D; Collins-Nakai R; Hoo JJ Clin Genet; 1986 Feb; 29(2):174-7. PubMed ID: 3955871 [TBL] [Abstract][Full Text] [Related]
16. [Partial trisomy of chromosome 1.46,XX dir. dup (1q) (q32-q44)]. Saitua G; Molina M; Pedro Arrate J; Ereño C; Delgado A Bol Med Hosp Infant Mex; 1986 May; 43(5):308-11. PubMed ID: 3730105 [No Abstract] [Full Text] [Related]
17. Features of Turner's and DiGeorge's syndromes in a child with an X;22 translocation. Pinto MR; Leite RP; Areias A J Med Genet; 1989 Dec; 26(12):778-80. PubMed ID: 2614798 [TBL] [Abstract][Full Text] [Related]
18. Primary pulmonary dysgenesis in velocardiofacial syndrome: a second patient. Cunningham ML; Perry RJ; Eby PR; Gibson RL; Opheim KE; Manning SC Am J Med Genet A; 2003 Aug; 121A(2):177-9. PubMed ID: 12910501 [No Abstract] [Full Text] [Related]
19. In situ hybridization and translocation breakpoint mapping. III. DiGeorge syndrome with partial monosomy of chromosome 22. Cannizzaro LA; Emanuel BS Cytogenet Cell Genet; 1985; 39(3):179-83. PubMed ID: 3930157 [TBL] [Abstract][Full Text] [Related]