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26. The use of a specific clinical history in counselling a family with the balanced translocation 46,XY,t(4;12)(p15.2;q21.3): viable offspring with partial monosomy 4p and trisomy 12q. Wilson CJ; Oei PT Clin Genet; 1998 Jul; 54(1):110-1. PubMed ID: 9727755 [No Abstract] [Full Text] [Related]
27. Trisomy 4p: five new observations and overview. Dallapiccola B; Mastroiacovo PP; Montali E; Sommer A Clin Genet; 1977 Dec; 12(6):344-56. PubMed ID: 563312 [TBL] [Abstract][Full Text] [Related]
28. Neu-Laxova syndrome: report of a case from Turkey. Kuseyri F; Bilge I; Bilgiç L; Apak MY Clin Genet; 1993 May; 43(5):267-9. PubMed ID: 8375108 [TBL] [Abstract][Full Text] [Related]
29. Double trisomy. Li S; Hassed S; Mulvihill JJ; Nair AK; Hopcus DJ Am J Med Genet A; 2004 Jan; 124A(1):96-8. PubMed ID: 14679595 [No Abstract] [Full Text] [Related]
30. [A newborn infant with the Bowen-Conradi syndrome; a fatal hereditary disorder]. Beemer FA; Gerards LJ Tijdschr Kindergeneeskd; 1982 Apr; 50(2):54-7. PubMed ID: 7123536 [No Abstract] [Full Text] [Related]
31. Trisomy 22 in a liveborn infant with multiple congenital anomalies. McPherson E; Stetka DG Am J Med Genet; 1990 May; 36(1):11-4. PubMed ID: 2333899 [TBL] [Abstract][Full Text] [Related]
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33. Molecular cytogenetic analysis of de novo dup(5)(q33.1q31.1) associated with abnormal perinatal findings. Chen CP; Lin SP; Chern SR; Lin CC; Li YC; Lee CC; Hsieh LJ; Chen WL; Wang W Prenat Diagn; 2006 Feb; 26(2):181-3. PubMed ID: 16470511 [No Abstract] [Full Text] [Related]
34. Full trisomy 22 in a malformed newborn female. Feret MA; Galán F; Aguilar MS; Serrano JL; Cidras M; Garcia R Ann Genet; 1991; 34(1):44-6. PubMed ID: 1952793 [TBL] [Abstract][Full Text] [Related]
35. Microcephaly and intracranial calcification: two new cases. Monastiri K; Salem N; Korbi S; Snoussi N Clin Genet; 1997 Feb; 51(2):142-3. PubMed ID: 9112011 [No Abstract] [Full Text] [Related]
36. Distal 10q trisomy syndrome with unusual cardiac and pulmonary abnormalities. Davies J; Jaffé A; Bush A J Med Genet; 1998 Jan; 35(1):72-4. PubMed ID: 9475101 [TBL] [Abstract][Full Text] [Related]
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38. Recurrent Galloway Mowat syndrome associated with abnormal prenatal sonographic findings. Chen CP; Lin SP; Chang TY; Tsai JD; Huang JK; Wang W Genet Couns; 2006; 17(1):87-9. PubMed ID: 16719284 [No Abstract] [Full Text] [Related]
39. Multiple abnormalities in a preterm infant with growth retardation. Cowett RM; Singer DB R I Med J (1976); 1984 May; 67(5):233-7. PubMed ID: 6588444 [No Abstract] [Full Text] [Related]
40. Two Cases with Ring Chromosome 13 at either End of the Phenotypic Spectrum. Çakmaklı S; Çankaya T; Gürsoy S; Koç A; Kırbıyık Ö; Kılıçarslan ÖA; Özer E; Erçal D; Bozkaya ÖG Cytogenet Genome Res; 2017; 153(4):175-180. PubMed ID: 29518772 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]