These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
22. Sonographically detected fetal and placental abnormalities associated with trisomy 16 confined to the placenta. A case report and review of the literature. Astner A; Schwinger E; Caliebe A; Jonat W; Gembruch U Prenat Diagn; 1998 Dec; 18(12):1308-15. PubMed ID: 9885025 [TBL] [Abstract][Full Text] [Related]
23. Maternal uniparental isodisomy for chromosome 14 detected prenatally. Ralph A; Scott F; Tiernan C; Caubere M; Kollegger S; Junio J; Roberts C; Ewen K; Slater HR Prenat Diagn; 1999 Jul; 19(7):681-4. PubMed ID: 10419621 [TBL] [Abstract][Full Text] [Related]
24. Maternal uniparental disomy 14 dissection of the phenotype with respect to rare autosomal recessively inherited traits, trisomy mosaicism, and genomic imprinting. Kotzot D Ann Genet; 2004; 47(3):251-60. PubMed ID: 15337470 [TBL] [Abstract][Full Text] [Related]
25. Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicism. Jones C; Booth C; Rita D; Jazmines L; Spiro R; McCulloch B; McCaskill C; Shaffer LG Prenat Diagn; 1995 Sep; 15(9):843-8. PubMed ID: 8559755 [TBL] [Abstract][Full Text] [Related]
26. Uniparental isodisomy due to duplication of chromosome 21 occurring in somatic cells monosomic for chromosome 21. Petersen MB; Bartsch O; Adelsberger PA; Mikkelsen M; Schwinger E; Antonarakis SE Genomics; 1992 Jun; 13(2):269-74. PubMed ID: 1351865 [TBL] [Abstract][Full Text] [Related]
27. Maternal uniparental disomy 16 and genetic counseling: new case and survey of published cases. Eggermann T; Curtis M; Zerres K; Hughes HE Genet Couns; 2004; 15(2):183-90. PubMed ID: 15287418 [TBL] [Abstract][Full Text] [Related]
28. Mosaicism for duplication 12q (12q13-->q24.2) in a dysmorphic male infant. Dixon JW; Costa T; Teshima IE J Med Genet; 1993 Jan; 30(1):70-2. PubMed ID: 8423612 [TBL] [Abstract][Full Text] [Related]
30. Mosaic paternal uniparental (iso)disomy for chromosome 20 associated with multiple anomalies. Venditti CP; Hunt P; Donnenfeld A; Zackai E; Spinner NB Am J Med Genet A; 2004 Jan; 124A(3):274-9. PubMed ID: 14708100 [TBL] [Abstract][Full Text] [Related]
31. Trisomy 18 with unilateral atypical ectrodactyly. Rogers RC Am J Med Genet; 1994 Jan; 49(1):125-7. PubMed ID: 8172239 [No Abstract] [Full Text] [Related]
32. Post-zygotic origin of complete maternal chromosome 7 isodisomy and consequent loss of placental PEG1/MEST expression. Miozzo M; Grati FR; Bulfamante G; Rossella F; Cribiù M; Radaelli T; Cassani B; Persico T; Cetin I; Pardi G; Simoni G Placenta; 2001 Nov; 22(10):813-21. PubMed ID: 11718568 [TBL] [Abstract][Full Text] [Related]
33. Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism. Christian SL; Smith AC; Macha M; Black SH; Elder FF; Johnson JM; Resta RG; Surti U; Suslak L; Verp MS; Ledbetter DH Prenat Diagn; 1996 Apr; 16(4):323-32. PubMed ID: 8734806 [TBL] [Abstract][Full Text] [Related]
34. A prenatal diagnosis of mosaic trisomy 5 reveals a postnatal complete uniparental disomy of chromosome 5 with multiple congenital anomalies. Reittinger AM; Helm BM; Boles DJ; Gadi IK; Schrier Vergano SA Am J Med Genet A; 2017 Sep; 173(9):2528-2533. PubMed ID: 28653809 [TBL] [Abstract][Full Text] [Related]
35. Maternal uniparental disomy 7--review and further delineation of the phenotype. Kotzot D; Balmer D; Baumer A; Chrzanowska K; Hamel BC; Ilyina H; Krajewska-Walasek M; Lurie IW; Otten BJ; Schoenle E; Tariverdian G; Schinzel A Eur J Pediatr; 2000 Apr; 159(4):247-56. PubMed ID: 10789928 [TBL] [Abstract][Full Text] [Related]
36. A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9. Wilkinson TA; James RS; Crolla JA; Cockwell AE; Campbell PL; Temple IK Prenat Diagn; 1996 Apr; 16(4):371-4. PubMed ID: 8734817 [TBL] [Abstract][Full Text] [Related]
37. Variable clinical expression of mosaic trisomy 16 in the newborn infant. Devi AS; Velinov M; Kamath MV; Eisenfeld L; Neu R; Ciarleglio L; Greenstein R; Benn P Am J Med Genet; 1993 Aug; 47(2):294-8. PubMed ID: 8213923 [TBL] [Abstract][Full Text] [Related]
38. Maternal UPD 20 in an infant from a pregnancy with mosaic trisomy 20. Salafsky IS; MacGregor SN; Claussen U; von Eggeling F Prenat Diagn; 2001 Oct; 21(10):860-3. PubMed ID: 11746130 [TBL] [Abstract][Full Text] [Related]
39. Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction. Chen CP; Chern SR; Chang TY; Lee CC; Chen LF; Tzen CY; Wang W; Lin CJ; Yang BP; Yang LS Prenat Diagn; 2003 Jan; 23(1):40-3. PubMed ID: 12533811 [TBL] [Abstract][Full Text] [Related]
40. Centromeric DNA break in a 10;16 reciprocal translocation associated with trisomy 16 confined placental mosaicism and maternal uniparental disomy for chromosome 16. Wang JC; Mamunes P; Kou SY; Schmidt J; Mao R; Hsu WT Am J Med Genet; 1998 Dec; 80(4):418-22. PubMed ID: 9856575 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]