248 related articles for article (PubMed ID: 16651677)
21. 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]
22. 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]
23. Identification of iso(18p) marker chromosome by fluorescence in situ hybridization with single-copy DNA probe.
Nakashima H; Hasegawa T; Sakai M; Inaba R; Imamura T
Jpn J Hum Genet; 1995 Jun; 40(2):185-8. PubMed ID: 7662998
[TBL] [Abstract][Full Text] [Related]
24. Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.
Blennow E; Nielsen KB; Telenius H; Carter NP; Kristoffersson U; Holmberg E; Gillberg C; Nordenskjöld M
Am J Med Genet; 1995 Jan; 55(1):85-94. PubMed ID: 7702104
[TBL] [Abstract][Full Text] [Related]
25. Clinical and cytogenetic manifestations of subtelomeric aberrations: Report of six cases.
Font-Montgomery E; Weaver DD; Walsh L; Christensen C; Thurston VC
Birth Defects Res A Clin Mol Teratol; 2004 Jun; 70(6):408-15. PubMed ID: 15211711
[TBL] [Abstract][Full Text] [Related]
26. [Tetrasomy 12p (Pallister-Killian syndrome): possible diagnosis before the age of a year].
Chrzanowska K; Fryns JP
J Genet Hum; 1989 Sep; 37(3):259-61. PubMed ID: 2625629
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Pallister-Killian Syndrome (PKS) as a Cause of Mental Retardation.
Shamdeen A; Meyer S; Gottschling S; Oehl-Jaschkowitz B; Gortner L; Shamdeen MG
Klin Padiatr; 2009; 221(2):97-9. PubMed ID: 19067289
[TBL] [Abstract][Full Text] [Related]
29. FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype.
Baroncini A; Rivieri F; Capucci A; Croci G; Franchi F; Sensi A; Battaglia P; Aiello V; Calzolari E
Eur J Med Genet; 2005; 48(4):388-96. PubMed ID: 16378923
[TBL] [Abstract][Full Text] [Related]
30. Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridization.
Darnaude MT; Diaz de Bustamante A; Cabello P; Vallcorba I
Ann Genet; 1996; 39(2):61-3. PubMed ID: 8766134
[TBL] [Abstract][Full Text] [Related]
31. Cytogenetic investigation of a child with a mosaic isochromosome 18q and ring 18q.
Souraty N; Sanlaville D; Chédid R; Le Lorc'h M; Maurin ML; Ghanem L; Maalouf S; Vekemans M; Mégarbané A
Eur J Med Genet; 2007; 50(5):379-85. PubMed ID: 17716964
[TBL] [Abstract][Full Text] [Related]
32. De novo partial duplication of 17p [dup(17)(p12----p11.2)]: clinical report.
Magenis RE; Brown MG; Allen L; Reiss J
Am J Med Genet; 1986 Jul; 24(3):415-20. PubMed ID: 2425620
[TBL] [Abstract][Full Text] [Related]
33. De novo mosaic ring chromosome 18 in a child with mental retardation, epilepsy and immunological problems.
Lo-Castro A; El-Malhany N; Galasso C; Verrotti A; Nardone AM; Postorivo D; Palmieri C; Curatolo P
Eur J Med Genet; 2011; 54(3):329-32. PubMed ID: 21333764
[TBL] [Abstract][Full Text] [Related]
34. An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.
Bremer A; Schoumans J; Nordenskjöld M; Anderlid BM; Giacobini M
Eur J Med Genet; 2009; 52(5):358-62. PubMed ID: 19576304
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. "Ring syndrome" involving chromosome 2 confirmed by FISH analysis using chromosome-specific subtelomeric probes.
Kosho T; Matsushima K; Sahashi T; Mitsui N; Fukushima Y; Sobajima H; Ohashi H
Genet Couns; 2005; 16(1):65-70. PubMed ID: 15844781
[TBL] [Abstract][Full Text] [Related]
37. Meiotic origin of two ring chromosomes 18 in a girl with developmental delay.
Baumer A; Giovannucci Uzielli ML; Guarducci S; Lapi E; Röthlisberger B; Schinzel A
Am J Med Genet; 2002 Nov; 113(1):101-4. PubMed ID: 12400074
[TBL] [Abstract][Full Text] [Related]
38. Characterization of a de novo balanced translocation in a patient with moderate mental retardation and dysmorphic features.
Haddad MR; Mignon-Ravix C; Cacciagli P; Mégarbané A; Villard L
Eur J Med Genet; 2009; 52(4):211-7. PubMed ID: 19379847
[TBL] [Abstract][Full Text] [Related]
39. Mental retardation and developmental delay due to mosaic chromosome 14q duplication.
Thapa R; Bhattacharya S; Ghosh A
J Dev Behav Pediatr; 2008 Dec; 29(6):541-2. PubMed ID: 19077851
[No Abstract] [Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
