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.
372 related articles for article (PubMed ID: 7528972)
1. 10p duplication characterized by fluorescence in situ hybridization. Wiktor A; Feldman GL; Kratkoczki P; Ditmars DM; Van Dyke DL Am J Med Genet; 1994 Sep; 52(3):315-8. PubMed ID: 7528972 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. Cytogenetic and molecular identification of a de novo direct duplication of the long arm of chromosome 4(q21.3-->q31.3). Jeziorowska A; Ciesla W; Houck GE; Yao XL; Harris MS; Truszczak B; Skorski M; Jakubowski L; Jenkins EC; Kaluzewski B Am J Med Genet; 1993 Apr; 46(1):83-7. PubMed ID: 7684191 [TBL] [Abstract][Full Text] [Related]
4. Detection of an unbalanced t(4;15) by FISH in a child with multiple congenital anomalies. Celep F; Acar H; Aynaci O; Aynaci FM; Karagüzel A Genet Couns; 2001; 12(4):319-26. PubMed ID: 11837600 [TBL] [Abstract][Full Text] [Related]
5. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate. Kobayashi J; Kimijima Y; Yamada S; Amagasa T; Saito-Ohara F J Craniomaxillofac Surg; 2000 Jun; 28(3):165-70. PubMed ID: 10964553 [TBL] [Abstract][Full Text] [Related]
6. Duplication of (2)(q11.1-q13.2) in a boy with mental retardation and cleft lip and palate: another clefting gene locus on proximal 2q? Riegel M; Schinzel A Am J Med Genet; 2002 Jul; 111(1):76-80. PubMed ID: 12124740 [TBL] [Abstract][Full Text] [Related]
7. Duplication 20p identified via fluorescent in situ hybridization. LeChien KA; McPherson E; Estop AM Am J Med Genet; 1994 Apr; 50(2):187-9. PubMed ID: 7516625 [TBL] [Abstract][Full Text] [Related]
8. Identification and molecular confirmation of a small chromosome 10q duplication [dir dup(10)(q24.2-->q24.3)] inherited from a mother mosaic for the abnormality. Tonk V; Schneider NR; Delgado MR; Mao J; Schultz RA Am J Med Genet; 1996 Jan; 61(1):16-20. PubMed ID: 8741911 [TBL] [Abstract][Full Text] [Related]
9. Lobar holoprosencephaly in 18pter deletion resulting from the karyotype 45,X,-18,der(8;18)t(8; 18)(pter;p11.21). Witters I; Balikova I; Cannie M; Devriendt K; De Catte L; Fryns JP Genet Couns; 2008; 19(4):443-6. PubMed ID: 19239091 [No Abstract] [Full Text] [Related]
10. Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13). Tschernigg M; Petek E; Leonhardtsberger A; Wagner K; Kroisel PM Genet Couns; 2002; 13(3):303-7. PubMed ID: 12416638 [TBL] [Abstract][Full Text] [Related]
11. De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder. Goumy C; Mihaescu M; Tchirkov A; Giollant M; Benier C; Francannet C; Jaffray JY; Geneix A; Vago P Genet Couns; 2006; 17(3):371-9. PubMed ID: 17100206 [TBL] [Abstract][Full Text] [Related]
12. A dysmorphic newborn infant with a complex rearrangement involving chromosomes 2, 4, and 6 detected by fluorescence in situ hybridization (FISH). Hoffman DJ; Punnett HH; Pyeritz RE Am J Perinatol; 2004 Feb; 21(2):69-71. PubMed ID: 15017469 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat. Qumsiyeh MB; Stevens CA Am J Med Genet; 1993 Sep; 47(3):387-91. PubMed ID: 8135287 [TBL] [Abstract][Full Text] [Related]
15. Detection of a subtle rearrangement of chromosome 22 using molecular techniques. Biesecker LG; Rosenberg M; Dziadzio L; Ledbetter DH; Ning Y; Sarneso C; Rosenbaum K Am J Med Genet; 1995 Sep; 58(4):389-94. PubMed ID: 8533859 [TBL] [Abstract][Full Text] [Related]
16. Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip--palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12)(q24;q24). Callier P; Faivre L; Marle N; Thauvin-Robinet C; Mosca AL; Masurel-Paulet A; Borgnon J; Falcon-Eicher S; Danino A; Malka G; Le Merrer M; Huet F; Mugneret F Eur J Med Genet; 2007; 50(6):455-64. PubMed ID: 17720646 [TBL] [Abstract][Full Text] [Related]
17. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features. Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292 [TBL] [Abstract][Full Text] [Related]
18. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies. Spikes AS; Hegmann K; Smith JL; Shaffer LG Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595 [TBL] [Abstract][Full Text] [Related]
19. Marker chromosome 21 identified by microdissection and FISH. Sun Y; Rubinstein J; Soukup S; Palmer CG Am J Med Genet; 1995 Mar; 56(2):151-4. PubMed ID: 7542834 [TBL] [Abstract][Full Text] [Related]