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251 related items for PubMed ID: 1466563
1. Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new cases. Poissonnier M, Turleau C, Olivier-Martin M, Milleret-Proyart MJ, Prieur M, Dubos M, Cabanis MO, Mugneret F, Blanc P, Noel L. Ann Genet; 1992; 35(3):146-51. PubMed ID: 1466563 [Abstract] [Full Text] [Related]
2. Distal deletion of the long arm of chromosome number 1 (q43-->qter) associated with severe mental retardation and a nonspecific dysmorphic syndrome. Ioan DM, Maximilian C, Kleczkowska A, Fryns JP. Ann Genet; 1992; 35(3):167-9. PubMed ID: 1466567 [Abstract] [Full Text] [Related]
3. Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome. Stratton RF, Dobyns WB, Greenberg F, DeSana JB, Moore C, Fidone G, Runge GH, Feldman P, Sekhon GS, Pauli RM. Am J Med Genet; 1986 Jul; 24(3):421-32. PubMed ID: 3728561 [Abstract] [Full Text] [Related]
4. Constitutional interstitial deletion of 17(p11.2) (Smith-Magenis syndrome): a clinically recognizable microdeletion syndrome. Report of two cases and review of the literature. Fischer H, Oswald HP, Duba HC, Doczy L, Simma B, Utermann G, Haas OA. Klin Padiatr; 1993 Jul; 205(3):162-6. PubMed ID: 8350589 [Abstract] [Full Text] [Related]
8. Interstitial deletion of the long arm of chromosome 18, del(18)(q12.2q21.1): a report of three cases of an autosomal deletion with a mild phenotype. Schinzel A, Binkert F, Lillington DM, Sands M, Stocks RJ, Lindenbaum RH, Matthews H, Sheridan H. J Med Genet; 1991 May; 28(5):352-5. PubMed ID: 1865477 [Abstract] [Full Text] [Related]
9. Moderate mental retardation and mild dysmorphic syndrome in proximal 7q interstitial deletion. Fryns JP, Kleczkowska A, Van den Berghe H. Ann Genet; 1987 May; 30(2):111-2. PubMed ID: 3499842 [Abstract] [Full Text] [Related]
11. Interstitial deletion of (17)(p11.2p11.2) in nine patients. Smith AC, McGavran L, Robinson J, Waldstein G, Macfarlane J, Zonona J, Reiss J, Lahr M, Allen L, Magenis E. Am J Med Genet; 1986 Jul; 24(3):393-414. PubMed ID: 2425619 [Abstract] [Full Text] [Related]
12. Periventricular heterotopia in a boy with interstitial deletion of chromosome 4p. Gawlik-Kuklinska K, Wierzba J, Wozniak A, Iliszko M, Debiec-Rychter M, Dubaniewicz-Wybieralska M, Limon J. Eur J Med Genet; 2008 Jul; 51(2):165-71. PubMed ID: 18243084 [Abstract] [Full Text] [Related]
17. Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28-->q31.3). Copelli S, del Rey G, Heinrich J, Coco R. Am J Med Genet; 1995 Jan 02; 55(1):77-9. PubMed ID: 7702102 [Abstract] [Full Text] [Related]
18. Interstitial deletion of a proximal 3p: a clinically recognisable syndrome. Lalli C, Galasso C, Lo Castro A, Nardone AM, Di Paolo A, Curatolo P. Brain Dev; 2007 Jun 02; 29(5):312-6. PubMed ID: 17125947 [Abstract] [Full Text] [Related]
19. Ring chromosome 17 in a mentally retarded boy. Qazi OH, Madahar C, Kanchanapoomi R, Giridharan R, Beller E. Ann Genet; 1979 Jun 02; 22(4):234-8. PubMed ID: 121681 [Abstract] [Full Text] [Related]
20. Interstitial deletion of the short arm of chromosome 8: report of a patient and review of the literature. Plomp AS, Schrander-Stumpel CT, Engelen JJ, Sijstermans JM, Loneus WH, Fryns JP. Genet Couns; 1995 Jun 02; 6(1):55-60. PubMed ID: 7794563 [Abstract] [Full Text] [Related] Page: [Next] [New Search]