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7. Genetic screening for maternal uniparental disomy of chromosome 7 in prenatal and postnatal growth retardation of unknown cause. Hannula K; Lipsanen-Nyman M; Kristo P; Kaitila I; Simola KO; Lenko HL; Tapanainen P; Holmberg C; Kere J Pediatrics; 2002 Mar; 109(3):441-8. PubMed ID: 11875139 [TBL] [Abstract][Full Text] [Related]
8. Sporadic occurrence of nondeletion Prader-Willi syndrome in two cases: a female with maternal uniparental disomy and a male with complex chromosomal rearrangement. Murthy SK; al-Nassar KE; Verghese L Nutrition; 1995; 11(5 Suppl):650-2. PubMed ID: 8748243 [TBL] [Abstract][Full Text] [Related]
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11. Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients. Eggermann T; Mergenthaler S; Eggermann K; Albers A; Linnemann K; Fusch C; Ranke MB; Wollmann HA J Med Genet; 2001 Feb; 38(2):86-9. PubMed ID: 11158171 [TBL] [Abstract][Full Text] [Related]
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13. Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation. Calounova G; Novotna D; Simandlova M; Havlovicova M; Zumrová A; Kocarek E; Sedlacek Z Neuro Endocrinol Lett; 2006 Oct; 27(5):579-85. PubMed ID: 17159828 [TBL] [Abstract][Full Text] [Related]
14. MECHANISMS IN ENDOCRINOLOGY: Novel genetic causes of short stature. Wit JM; Oostdijk W; Losekoot M; van Duyvenvoorde HA; Ruivenkamp CA; Kant SG Eur J Endocrinol; 2016 Apr; 174(4):R145-73. PubMed ID: 26578640 [TBL] [Abstract][Full Text] [Related]
15. Maternal uniparental heterodisomy of chromosome 14: chromosomal mechanism and clinical follow up. Sanlaville D; Aubry MC; Dumez Y; Nolen MC; Amiel J; Pinson MP; Lyonnet S; Munnich A; Vekemans M; Morichon-Delvallez N J Med Genet; 2000 Jul; 37(7):525-8. PubMed ID: 10882756 [TBL] [Abstract][Full Text] [Related]
16. Early embryonic failure associated with uniparental disomy for human chromosome 21. Henderson DJ; Sherman LS; Loughna SC; Bennett PR; Moore GE Hum Mol Genet; 1994 Aug; 3(8):1373-6. PubMed ID: 7987317 [TBL] [Abstract][Full Text] [Related]
17. Silver-Russell syndrome and exclusion of uniparental disomy. Ayala-Madrigal ML; Shaffer LG; Ramírez-Dueñas ML Clin Genet; 1996 Dec; 50(6):494-7. PubMed ID: 9147881 [TBL] [Abstract][Full Text] [Related]
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