136 related articles for article (PubMed ID: 8825933)
21. Prenatal diagnosis of holoprosencephaly (HPE) in a fetus with a recombinant (18)dup(18q)inv(18)(p11.31q11.2)mat.
Leonard NJ; Tomkins DJ; Demianczuk N
Prenat Diagn; 2000 Dec; 20(12):947-9. PubMed ID: 11113905
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Prenatal detection of monosomy 18p and trisomy 18q mosaicism with unexpected fetal phenotype.
Sutton SD; Ridler MA
J Med Genet; 1986 Jun; 23(3):258-9. PubMed ID: 3723556
[TBL] [Abstract][Full Text] [Related]
24. [Isochromosome long arm 18].
Rodiere M; Donadio D; Emberger JM; Astruc J; Brunel D
Ann Pediatr (Paris); 1977 Sep; 24(8-9):611-6. PubMed ID: 16211915
[No Abstract] [Full Text] [Related]
25. Application of interphase fluorescence in situ hybridization to uncultured amniocytes for differential diagnosis of pseudomosaicism from true mosaicism in mosaic isochromosome 20q detected at amniocentesis.
Chen CP; Chern SR; Wu PS; Su JW; Chen YT; Chen LF; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2013 Sep; 52(3):450-3. PubMed ID: 24075394
[No Abstract] [Full Text] [Related]
26. Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques.
de Pater JM; Govaerts LC; de Man SA; van der Sijs-Bos CJ; Christiaens GC; van Dam WM; Loneus WH; Engelen JJ
Prenat Diagn; 2003 Sep; 23(9):747-51. PubMed ID: 12975787
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. DNA studies of mono- and pseudodicentric isochromosomes 18q.
Bugge M; Brandt CA; Petersen MB
Am J Med Genet A; 2004 Jun; 127A(3):230-3. PubMed ID: 15150771
[TBL] [Abstract][Full Text] [Related]
29. Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion.
Prontera P; Aiello V; Toschi M; Turci A; Gruppioni R; Buldrini B; Zago S; Bonfatti A; Donti E; Calzolari E; Sensi A
Genet Couns; 2007; 18(3):309-15. PubMed ID: 18019372
[TBL] [Abstract][Full Text] [Related]
30. Turner syndrome isochromosome karyotype correlates with decreased dental crown width.
Rizell S; Barrenäs ML; Andlin-Sobocki A; Stecksén-Blicks C; Kjellberg H
Eur J Orthod; 2012 Apr; 34(2):213-8. PubMed ID: 21303812
[TBL] [Abstract][Full Text] [Related]
31. True fetal mosaicism of an isochromosome of the long arm of a chromosome 20: the dilemma persists.
Pfeiffer RA; Ulmer R; Rauch A; Trautmann U; Beinder E; Rupprecht T; Mayer U; Steinkirchner B; Wündisch GF
Prenat Diagn; 1997 Dec; 17(12):1171-5. PubMed ID: 9467815
[TBL] [Abstract][Full Text] [Related]
32. Isochromosome 5p mosaicism at prenatal diagnosis: observations and outcomes in six cases at chorionic villus sampling and one at amniocentesis.
Wilson SC; Susman M; Bain S; Wohlferd M; Van Dyke D; Daniel A; White B; Gardner RJ
Prenat Diagn; 2002 Aug; 22(8):681-5. PubMed ID: 12210576
[TBL] [Abstract][Full Text] [Related]
33. Pregnancy and postnatal outcome of mosaic isochromosome 20q.
Robinson WP; McGillivray B; Friedman JM
Prenat Diagn; 2007 Feb; 27(2):143-5. PubMed ID: 17191261
[TBL] [Abstract][Full Text] [Related]
34. Prenatal diagnosis of 18q-syndrome: a case of fetal mosaicism with a normal karyotype in chorionic villi.
Anselem O; Bazin A; Mechler C; Blin G; Garel C; Aboura A; Moutard ML; Mandelbrot L
Fetal Diagn Ther; 2010; 28(3):180-5. PubMed ID: 20829580
[TBL] [Abstract][Full Text] [Related]
35. Prenatal detection of isochromosome 21 by QF-PCR. A comparison between FISH and traditional karyotyping.
Gole L; Lian NB; Lian NP; Rauff M; Biswas A; Choolani M
Fetal Diagn Ther; 2008; 24(1):47-50. PubMed ID: 18504381
[TBL] [Abstract][Full Text] [Related]
36. Identification of complex chromosome 18 rearrangements by FISH and array CGH in two patients with apparent isochromosome 18q.
Breman AM; Probst FJ; Blazo MA; Schaaf CP; Roney EK; Craigen WJ; Bacino CA; Cheung SW
Am J Med Genet A; 2011 Jun; 155A(6):1465-8. PubMed ID: 21567909
[No Abstract] [Full Text] [Related]
37. Discordant prenatal diagnosis of trisomy 21 due to mosaic structural rearrangements of chromosome 21.
Brisset S; Aboura A; Audibert F; Costa JM; L'Herminé AC; Gautier V; Frydman R; Tachdjian G
Prenat Diagn; 2003 Jun; 23(6):461-9. PubMed ID: 12813759
[TBL] [Abstract][Full Text] [Related]
38. An additional report of prenatal detection of mosaic isochromosome 20q at amniocentesis.
Storto P; Diehn T
Prenat Diagn; 1997 Jan; 17(1):89-90. PubMed ID: 9021836
[No Abstract] [Full Text] [Related]
39. Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1.
Chen CP; Hsieh CH; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Lee CC; Wang W
Taiwan J Obstet Gynecol; 2017 Dec; 56(6):847-851. PubMed ID: 29241933
[TBL] [Abstract][Full Text] [Related]
40. 46,XY,18q+/46,XY,18q- mosaicism in a fragile X prenatal diagnosis.
Rodriguez-Revenga L; Badenas C; Madrigal I; Sánchez A; Soler A; Carrió A; Milà M
Prenat Diagn; 2005 Jun; 25(6):448-50. PubMed ID: 15966059
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
