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Journal Abstract Search
156 related items for PubMed ID: 6873945
1. Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation. Franceschini P, Cirillo Silengo M, Davi G, Bianco R, Biagioli M. Hum Genet; 1983; 64(1):98. PubMed ID: 6873945 [No Abstract] [Full Text] [Related]
3. Interstitial deletion of chromosome 1 (q23-q25). Report of a case. Silengo MC, Davi GF, Bianco R, Biagioli M, Guala A, Franceschini P, Novelli G. Clin Genet; 1984 Jun; 25(6):549-52. PubMed ID: 6587954 [Abstract] [Full Text] [Related]
4. Interstitial deletion of the short arm of chromosome 4. Ray M, Evans J, Rockman-Greenberg C, Wickstrom D. J Med Genet; 1984 Jun; 21(3):223-5. PubMed ID: 6748021 [Abstract] [Full Text] [Related]
6. Interstitial deletion of the long arm of chromosome 2: a case report and review of the literature. Takahashi Y, Narahara K, Kikkawa K, Wakita Y, Kimura S, Murakami M, Kasai R, Kimoto H. Jinrui Idengaku Zasshi; 1985 Dec; 30(4):297-305. PubMed ID: 3869838 [No Abstract] [Full Text] [Related]
7. Interstitial deletion of the long arm of chromosome 4 in a patient with mental retardation and abnormal phenotype. del Valle Torrado M, Labarta JD, Migliorini AM. J Med Genet; 1982 Dec; 19(6):477. PubMed ID: 6185682 [No Abstract] [Full Text] [Related]
8. Terminal long-arm deletion of chromosome 1 in a male infant. Dignan PS, Soukup S. Hum Genet; 1979 Apr 27; 48(2):151-6. PubMed ID: 457139 [Abstract] [Full Text] [Related]
9. Deletion of the short arm of chromosome 20. Vianna-Morgante AM, Richieri-Costa A, Rosenberg C. Clin Genet; 1987 Jun 27; 31(6):406-9. PubMed ID: 3621644 [Abstract] [Full Text] [Related]
10. Terminal deletion with stable acentric fragment of 1q in a child with congenital malformations. Kucerová M, Polívková Z, Dluholucký S, Kvasnicová M. Am J Hum Genet; 1983 Jan 27; 35(1):91-5. PubMed ID: 6823976 [Abstract] [Full Text] [Related]
11. De novo interstitial deletion del(1)(p21p32). Bene M, Duca-Marinescu A, Ioan D, Maximilian C. J Med Genet; 1979 Aug 27; 16(4):323-7. PubMed ID: 490590 [Abstract] [Full Text] [Related]
12. Partial deletion of 1q, following a pericentric inversion, in a boy with multiple minor morphologic anomalies and mental retardation. Schwanitz G, Schmid P, Hägele C, Daffner HW, Grosse KP. Acta Genet Med Gemellol (Roma); 1977 Aug 27; 26(2):173-5. PubMed ID: 596113 [Abstract] [Full Text] [Related]
13. Interstitial deletion of the long arm of chromosome no. 5 in two unrelated children with congenital anomalies and mental retardation. Silengo MC, Luzzatti L, Centerwall WR, Costello JM, Parslow M. Clin Genet; 1981 Mar 27; 19(3):174-80. PubMed ID: 7273460 [Abstract] [Full Text] [Related]
14. De novo direct tandem duplication of the proximal long arm of chromosome 2: 46,XX,dir dup(2)(q11 X 2q14 X 2). Mu Y, Van Dyke DL, Weiss L, Olgac S. J Med Genet; 1984 Feb 27; 21(1):57-8. PubMed ID: 6694186 [Abstract] [Full Text] [Related]
16. Interstitial deletion of the short arm of chromosome 10 del(10)(p11.2p12.32) in a patient with congenital heart disease, minor dysmorphism, and mental retardation. Behjati F, Shafeghati Y, Kahrizi K, Firouzabadi SG, Najmabadi H, Dixon N, Davies AF. Am J Med Genet A; 2008 Dec 15; 146A(24):3223-6. PubMed ID: 19012333 [No Abstract] [Full Text] [Related]
17. Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15). Stoll C, Levy J, Roth MP. J Med Genet; 1980 Dec 15; 17(6):486-7. PubMed ID: 7205434 [Abstract] [Full Text] [Related]
18. [Familial translocation t(3;22) detected in a carrier child with mental retardation and other abnormalities]. Gregori Romero M, Gil Benso R, López Ginés C, Pellín Pérez A, Barberá Guillem E. An Esp Pediatr; 1984 Oct 31; 21(6):593-6. PubMed ID: 6524770 [Abstract] [Full Text] [Related]
19. Cat-like cry and mental retardation owing to 7q interstitial deletion (7q22 leads to 7q32). Abuelo DN, Padre-Mendoza T. J Med Genet; 1982 Dec 31; 19(6):473-6. PubMed ID: 7154049 [Abstract] [Full Text] [Related]
20. Interstitial deletion of the long arm of chromosome 3. Martsolf JT, Ray M. Ann Genet; 1983 Dec 31; 26(2):98-9. PubMed ID: 6604494 [Abstract] [Full Text] [Related] Page: [Next] [New Search]