79 related articles for article (PubMed ID: 12239721)
21. Larsen-like phenotype associated with partial trisomy 3p and monosomy 5p.
Goumy C; Beaufrère AM; Tchirkov A; Gouas L; Gaspard F; Giollant M; Roucaute T; Veronèse L; Lemery D; Vago P
Prenat Diagn; 2008 Feb; 28(2):131-4. PubMed ID: 18236428
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Partial trisomy 11q syndrome (11q23.1-->11qter) due to de novo t (11q; 13q) detected by multicolor fluorescence in situ hybridisation.
Utine GE; Thoelen R; Peeters H; Vermeesch J; Fryns JP
Genet Couns; 2005; 16(3):291-5. PubMed ID: 16259326
[TBL] [Abstract][Full Text] [Related]
24. [A case of acute promyelocytic leukemia with variant t(5;17) and trisomy 22].
Qiu HR; Li JY; Miao KR; Wang R; Zhang JF; Xu W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Aug; 25(4):430-3. PubMed ID: 18683144
[TBL] [Abstract][Full Text] [Related]
25. Trisomy 1q43 syndrome: a consistent phenotype with macrocephaly, characteristic face, developmental delay and cardiac anomalies.
Morava E; Jackson KE; Tsien F; Marble MR
Genet Couns; 2004; 15(4):449-53. PubMed ID: 15658621
[TBL] [Abstract][Full Text] [Related]
26. High resolution microarray CGH and MLPA analysis for improved genotype/phenotype evaluation of two childhood genetic disorder cases: ring chromosome 19 and partial duplication 2q.
Hermsen MA; Tijssen M; Acero IH; Meijer GA; Ylstra B; Toral JF
Eur J Med Genet; 2005; 48(3):310-8. PubMed ID: 16179226
[TBL] [Abstract][Full Text] [Related]
27. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
Liang DS; Wu LQ; Cai F; Xia K; Long ZG; Pan Q; Dai HP; Xia JH
Yi Chuan Xue Bao; 2005 Feb; 32(2):124-9. PubMed ID: 15759858
[TBL] [Abstract][Full Text] [Related]
28. Partial trisomy of 7q: case report and literature review.
Scelsa B; Bedeschi FM; Guerneri S; Lalatta F; Introvini P
J Child Neurol; 2008 May; 23(5):572-9. PubMed ID: 18056692
[TBL] [Abstract][Full Text] [Related]
29. First report of a partial trisomy 3q12-q23 de novo--FISH breakpoint determination and phenotypic characterization.
Gamerdinger U; Bosse K; Eggermann T; Kalscheuer V; Schwanitz G; Engels H
Eur J Med Genet; 2006; 49(3):225-34. PubMed ID: 16762824
[TBL] [Abstract][Full Text] [Related]
30. Constitutional partial 1q trisomy mosaicism and Wilms tumor.
Mark HF; Wyandt H; Pan A; Milunsky JM
Cancer Genet Cytogenet; 2005 Oct; 162(2):166-71. PubMed ID: 16213366
[TBL] [Abstract][Full Text] [Related]
31. Report of a patient with a trisomy of chromosome region 20q11.2-->20q12 and characterization with FISH.
Wanderley HY; Schrander-Stumpel CT; Visser MO; Van Maanen-Op Het Roodt EA; Loneus WH; Engelen JJ
Genet Couns; 2005; 16(3):277-82. PubMed ID: 16259325
[TBL] [Abstract][Full Text] [Related]
32. A case of trisomy 12 mosaicism with pituitary malformation and polycystic ovary syndrome.
Boulard S; Diene G; Barat R; Oliver I; Pienkowski C; Lacombe D; Vincent MC; Bourrouillou G; Tauber M
Genet Couns; 2006; 17(2):173-83. PubMed ID: 16970035
[TBL] [Abstract][Full Text] [Related]
33. Partial proximal trisomy 10q syndrome: a new case.
Nucaro A; Faedda A; Cao A; Boccone L
Genet Couns; 2002; 13(4):411-6. PubMed ID: 12558111
[TBL] [Abstract][Full Text] [Related]
34. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
El-Ruby M; Hemly NA; Zaki MS
Genet Couns; 2007; 18(2):217-26. PubMed ID: 17710874
[TBL] [Abstract][Full Text] [Related]
35. A case of an interstitial tandem direct duplication of long arm of chromosome 4: 46, XY, dup (4) (q25q31.3) de novo.
Muraki K; Katano R; Hiraki Y; Ueda K; Fujita H
Hiroshima J Med Sci; 1997 Sep; 46(3):105-8. PubMed ID: 9353971
[TBL] [Abstract][Full Text] [Related]
36. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.
Zaki MS; Kamel AA; El-Ruby M
Genet Couns; 2005; 16(4):393-402. PubMed ID: 16440882
[TBL] [Abstract][Full Text] [Related]
37. Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly.
Dobyns WB; Stratton RF; Greenberg F
Am J Med Genet; 1984 Jul; 18(3):509-26. PubMed ID: 6476009
[TBL] [Abstract][Full Text] [Related]
38. Hidden chromosome 8 abnormalities detected by FISH in adult primary myelodysplastic syndromes.
Panani AD; Pappa V
In Vivo; 2005; 19(6):979-81. PubMed ID: 16277010
[TBL] [Abstract][Full Text] [Related]
39. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
[TBL] [Abstract][Full Text] [Related]
40. M-FISH applications in clinical genetics.
Cetin Z; Berker Karaüzüm S; Yakut S; Mihçi E; Baumer A; Wey E; Taçoy S; Bağci G; Lüleci G
Genet Couns; 2005; 16(3):257-68. PubMed ID: 16259323
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
