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3. Absence of IgA and growth hormone deficiency associated with short arm deletion of chromosome 18. Leisti J; Leisti S; Perheentupa J; Savilahti E; Aula P Arch Dis Child; 1973 Apr; 48(4):320-2. PubMed ID: 4705937 [No Abstract] [Full Text] [Related]
4. Short-arm deletion, chromosome 4, (4p-), a syndrome? Taylor AI; Challacombe DN; Howlett RM Ann Hum Genet; 1970 Oct; 34(2):137-44. PubMed ID: 5493842 [No Abstract] [Full Text] [Related]
5. A mentally retarded child convulsions, agenesis of the corpus callosum, and a translocation involving chromosomes 2 and the B group. Mantle DJ; Mitchell P; Kucheria K; Wilson J J Med Genet; 1969 Dec; 6(4):435-7. PubMed ID: 5365953 [No Abstract] [Full Text] [Related]
6. A patient with a short arm deletion of chromosome 18 (46,XY,18p-). Weiss L; Mayeda K J Med Genet; 1969 Jun; 6(2):216-9. PubMed ID: 5801470 [No Abstract] [Full Text] [Related]
8. Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+). Wyandt HE; Hecht F; Lovrien EW; Stewart RE Cytogenetics; 1971; 10(6):413-26. PubMed ID: 5146418 [No Abstract] [Full Text] [Related]
9. Short arm deletion of chromosome 14. Emerit I; Noel B; Thiriet M; Loubon M; Quack B Humangenetik; 1972; 15(1):33-8. PubMed ID: 5046906 [No Abstract] [Full Text] [Related]
10. A short, retarded child with a deletion of the short arm of chromosome 18 (18p-). Parker CE; Donnell GN; Mavalwala J; Hurst N; Derencsenyi A Clin Pediatr (Phila); 1973 Jan; 12(1):42-6. PubMed ID: 4345621 [No Abstract] [Full Text] [Related]
11. [The clinical features of the 18 q-syndrome (author's transl)]. Feichtinger C; Glatzl J Wien Klin Wochenschr; 1974 Aug; 86(15):441-4. PubMed ID: 4605988 [No Abstract] [Full Text] [Related]
12. A structurally abnormal chromosome (46,XX,?17p+) associated with mental deficiency and congenital malformations. Ricci N; Dallapiccola B; Ventimiglia B J Med Genet; 1968 Sep; 5(3):220-3. PubMed ID: 5708027 [No Abstract] [Full Text] [Related]
13. A mentally retarded child with a translocation involving chromosomes 12 and 19. Histinx TW; Gabreƫls FJ; Rutten FJ; Korten II; Scheres JM; Joosten EM J Med Genet; 1975 Jun; 12(2):207-10. PubMed ID: 1142383 [TBL] [Abstract][Full Text] [Related]
14. Agenesis of the corpus callosum with mosaicism 46,XY/47,XY, extra ring chromosome. Zamboni G; Bernardi F; Danesino C; del Majno UM; Beghini G; Dalla Bernardina B J Med Genet; 1980 Feb; 17(1):59-61. PubMed ID: 7365765 [TBL] [Abstract][Full Text] [Related]
15. Ring chromosome 18 in a patient with multiple anomalies. Palmer CG; Fareed N; Merritt AD J Med Genet; 1967 Jun; 4(2):117-23. PubMed ID: 5619991 [No Abstract] [Full Text] [Related]
16. An extra small metacentric chromosome in association with multiple congenital abnormalities. Finley WH; Finley SC; Monsky D J Med Genet; 1971 Sep; 8(3):381-3. PubMed ID: 5097148 [No Abstract] [Full Text] [Related]
17. Cytogenetics in mentally defective children with anomalies: a controlled study. Summitt RL J Pediatr; 1969 Jan; 74(1):58-66. PubMed ID: 5782825 [No Abstract] [Full Text] [Related]
18. Ring chromosome 14 complicated with complex partial seizures and hypoplastic corpus callosum. Ono J; Nishiike K; Imai K; Otani K; Okada S Pediatr Neurol; 1999 Jan; 20(1):70-2. PubMed ID: 10029266 [TBL] [Abstract][Full Text] [Related]
19. Duplication deficiency syndrome in familial translocation (2q-;5p+). Bijlsma JB; de France H; Bleeker-Wagemakers EM Humangenetik; 1971; 12(2):110-22. PubMed ID: 5568729 [No Abstract] [Full Text] [Related]