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26. Ring chromosome 21 in the mother and 21/21 translocation in the fetus: karyotype: 45,XX,-21,-21,+t(21;21)(p11;q11). Fryns JP, Kleczkowska A. Ann Genet; 1987; 30(2):109-10. PubMed ID: 3499841 [Abstract] [Full Text] [Related]
28. Complex rearrangements of chromosome 15 in two patients with mild/atypical Prader Willi syndrome. Salavoura K, Kolialexi A, Sofocleous C, Kalaitzidaki M, Pampanos A, Kitsiou S, Mavrou A. Genet Couns; 2008; 19(2):219-24. PubMed ID: 18618997 [Abstract] [Full Text] [Related]
29. Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13. Eliez S, Morris MA, Dahoun-Hadorn S, DeLozier-Blanchet CD, Gos A, Sizonenko P, Antonarakis SE. Am J Med Genet; 1997 Jun 13; 70(3):222-8. PubMed ID: 9188657 [Abstract] [Full Text] [Related]
32. Pseudodicentric 22;Y translocation transmitted through four generations of a large family without phenotypic repercussion. Morales C, Soler A, Bruguera J, Madrigal I, Alsius M, Obon M, Margarit E, Sánchez A. Cytogenet Genome Res; 2007 Jun 13; 116(4):319-23. PubMed ID: 17431332 [Abstract] [Full Text] [Related]
33. Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocations. Mignon-Ravix C, Depetris D, Luciani JJ, Cuoco C, Krajewska-Walasek M, Missirian C, Collignon P, Delobel B, Croquette MF, Moncla A, Kroisel PM, Mattei MG. Eur J Hum Genet; 2007 Apr 13; 15(4):432-40. PubMed ID: 17264869 [Abstract] [Full Text] [Related]
34. Familial robertsonian translocation 15;21 and rare paracentric inv(21): unexpected re-inversion in a child with translocation trisomy 21. Mau UA, Petruch UR, Kaiser P, Eggermann T. Eur J Hum Genet; 2000 Nov 13; 8(11):815-9. PubMed ID: 11093270 [Abstract] [Full Text] [Related]
35. [Uniparental disomy: a review of causes and clinical sequelae]. Engel E. Ann Genet; 1995 Nov 13; 38(3):113-36. PubMed ID: 8540683 [Abstract] [Full Text] [Related]
36. A 15p+ variant shown to be a t(Y;15) with fluorescence in situ hybridisation. Neumann AA, Robson LG, Smith A. Ann Genet; 1992 Nov 13; 35(4):227-30. PubMed ID: 1296520 [Abstract] [Full Text] [Related]
37. A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15. Giardina E, Peconi C, Cascella R, Sinibaldi C, Nardone AM, Novelli G. Electrophoresis; 2008 Dec 13; 29(23):4775-9. PubMed ID: 19053076 [Abstract] [Full Text] [Related]
38. Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15). Varela MC, Lopes GM, Koiffmann CP. Ann Genet; 2004 Dec 13; 47(3):267-73. PubMed ID: 15337472 [Abstract] [Full Text] [Related]