212 related articles for article (PubMed ID: 10327251)
1. Mild dysmorphic signs in two male sibs with partial trisomy 2q32.1-->q35 due to maternal ins(14;2) translocation.
Lukusa T; Devriendt K; Jaeken J; Fryns JP
Clin Dysmorphol; 1999 Jan; 8(1):47-51. PubMed ID: 10327251
[TBL] [Abstract][Full Text] [Related]
2. Two sibs with partial trisomy 2q.
Barnicoat AJ; Abusaad I; Mackie CM; Robards MF
Am J Med Genet; 1997 May; 70(2):166-70. PubMed ID: 9128937
[TBL] [Abstract][Full Text] [Related]
3. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A
Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413
[TBL] [Abstract][Full Text] [Related]
4. Partial trisomy 14q due to maternal t(4;14)(p16;q32) in a dysmorphic newborn.
Dundar M; Uzak A; Saatci C; Akalin H
Genet Couns; 2011; 22(3):287-92. PubMed ID: 22029170
[TBL] [Abstract][Full Text] [Related]
5. Partial trisomy 18(q11 leads to qter) in an infant and aborted fetus resulting from a balanced paternal translocation t(13;18)(q32:q11).
Rosenmann A; Isacson M; Cohen R; Segal M; Cohen MM
Ann Genet; 1978 Mar; 21(1):60-4. PubMed ID: 308346
[TBL] [Abstract][Full Text] [Related]
6. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
Aglan MS; Kamel AK; Helmy NA
Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
[TBL] [Abstract][Full Text] [Related]
7. Precocious puberty associated with partial trisomy 18q and monosomy 11q.
Mutesa L; Hellin AC; Jamar M; Pierquin G; Bours V; Verloes A
Genet Couns; 2007; 18(2):201-7. PubMed ID: 17710872
[TBL] [Abstract][Full Text] [Related]
8. Familial translocation 2;17 with partial trisomy 2q32 leads to 2qter.
Giliberti P; Celona A; Della Pietra M; De Masi RV; Fioretti G; Pagano L; Renda S; Vetrella A; Ventruto V
Ann Genet; 1980; 23(4):249-50. PubMed ID: 6971607
[TBL] [Abstract][Full Text] [Related]
9. Duplication 2q33 leads to 2q37 due to paternal ins (12;2) translocation.
Dennis NR; Neu RL; Bannerman RM
Am J Med Genet; 1978; 1(3):271-7. PubMed ID: 677166
[TBL] [Abstract][Full Text] [Related]
10. Brief cytogenetic report on maternal translocation t(7;9) (p22:p13): two sibs with duplication 9p and one sib with the balanced translocation.
Wajntal A; Gonzalez CH; Koiffmann CP; de Souza DH
Am J Med Genet; 1985 Feb; 20(2):265-9. PubMed ID: 3976719
[TBL] [Abstract][Full Text] [Related]
11. [Genetics of partial trisomies. I. Trisomy 2q].
Lur'e IV; Rumiantseva NV; Podleshchuk LV; Kaurov BA; Zaletaev DV
Genetika; 1986 Jun; 22(6):1033-9. PubMed ID: 3732802
[TBL] [Abstract][Full Text] [Related]
12. Atypical manifestations of two cases of trisomy 9 syndrome: rethinking development delay.
Saneto RP; Applegate KE; Frankel DG
Am J Med Genet; 1998 Oct; 80(1):42-5. PubMed ID: 9800910
[TBL] [Abstract][Full Text] [Related]
13. Partial trisomy 17p12pter, associated with pre and postnatal growth retardation, dysmorphic facial and digital features, developmental delay, and signs of HMSN1 in early childhood.
Vogt J; Hill S; Brueton L
Eur J Med Genet; 2006; 49(5):439-43. PubMed ID: 16488202
[No Abstract] [Full Text] [Related]
14. Partial duplication 8q12----q21.2 in two sibs with maternally derived insertional and reciprocal translocations: case reports and review of partial duplications of chromosome 8.
Walker AP; Bocian M
Am J Med Genet; 1987 May; 27(1):3-22. PubMed ID: 3300332
[TBL] [Abstract][Full Text] [Related]
15. Family with partial monosomy 10p and trisomy 10p.
Hon E; Chapman C; Gunn TR
Am J Med Genet; 1995 Mar; 56(2):136-40. PubMed ID: 7625434
[TBL] [Abstract][Full Text] [Related]
16. Molecular Delineation of Partial Trisomy 14q and Partial Trisomy 12p in a Patient with Dysmorphic Features, Heart Defect and Developmental Delay.
Bose D; Krishnamurthy V; Venkatesh KS; Aiyaz M; Shetty M; Rao SN; Kutty AV
Cytogenet Genome Res; 2015; 145(1):14-8. PubMed ID: 25896599
[TBL] [Abstract][Full Text] [Related]
17. Trisomy 20q caused by der(4) t(4;20) (q35;q13.1): report of a new patient and review of the literature.
Plotner PL; Smith JL; Northrup H
Am J Med Genet; 2002 Jul; 111(1):71-5. PubMed ID: 12124739
[TBL] [Abstract][Full Text] [Related]
18. Partial 3q trisomy due to an unbalanced 3/10 translocation.
Blumberg B; Moore R; Mohandas T
Am J Med Genet; 1980; 7(3):335-9. PubMed ID: 7468658
[TBL] [Abstract][Full Text] [Related]
19. 2q35qter duplication syndrome: phenotypic definition.
Grammatico P; Di Rosa C; Rinaldi R; Roccella M; Cupilari F; Sbezzi T; Del Porto G
Genet Couns; 1997; 8(4):327-34. PubMed ID: 9457503
[TBL] [Abstract][Full Text] [Related]
20. [Syndrome of congenital malformations and dysmorphic features in a newborn with partial trisomy 16q due to maternal translocation t(9;16)(p24;q13)].
Luberda-Zapaśnik J; Midro AT; Szwałkiewicz-Warowicka E
Pediatr Pol; 1995 Sep; 70(9):769-73. PubMed ID: 8657511
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
