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6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. 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]
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. 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]
18. Velocardiofacial syndrome with a rare t(2;22). Huber J; Rainho CA; Gomes MV; Santos SA; Ramos ES Clin Dysmorphol; 2007 Jul; 16(3):181-183. PubMed ID: 17551333 [TBL] [Abstract][Full Text] [Related]
19. Molecular studies of DiGeorge syndrome. Fibison WJ; Budarf M; McDermid H; Greenberg F; Emanuel BS Am J Hum Genet; 1990 May; 46(5):888-95. PubMed ID: 2339689 [TBL] [Abstract][Full Text] [Related]
20. Detection of an atypical 22q11 deletion that has no overlap with the DiGeorge syndrome critical region. O'Donnell H; McKeown C; Gould C; Morrow B; Scambler P Am J Hum Genet; 1997 Jun; 60(6):1544-8. PubMed ID: 9199579 [No Abstract] [Full Text] [Related] [Next] [New Search]