Soler A - Search Results

1

Detection of balanced chromosome rearrangements in 445 couples with repeated abortion and cytogenetic prenatal testing in carriers.

Fortuny A, Carrio A, Soler A, Cararach J, Fuster J, Salami C. Fortuny A, et al. Among authors: soler a. Fertil Steril. 1988 May;49(5):774-9. doi: 10.1016/s0015-0282(16)59882-3. Fertil Steril. 1988. PMID: 3360167 Free article.

2

Unusual segregation for 11q;22q parental translocation in a triplet pregnancy: prenatal diagnosis in chorionic villi and amniotic fluid.

Soler A, Carrio A, Perez-Vidal MT, Borrell A, Fortuny A. Soler A, et al. Prenat Diagn. 1993 Feb;13(2):137-41. doi: 10.1002/pd.1970130209. Prenat Diagn. 1993. PMID: 8464833

3

Recombination in a male carrier of two reciprocal translocations involving chromosomes 14, 14', 15, and 21 leading to balanced and unbalanced rearrangements in offspring.

Soler A, Sánchez A, Carrió A, Badenas C, Milà M, Margarit E, Borrell A. Soler A, et al. Am J Med Genet A. 2005 Apr 30;134(3):309-14. doi: 10.1002/ajmg.a.30640. Am J Med Genet A. 2005. PMID: 15732062 Review.

4

Chorionic villus sampling by biopsy forceps. Results of 1580 procedures from a single centre.

Fortuny A, Borrell A, Soler A, Casals E, Costa D, Carrio A, Puerto B, Seres A, Cararach J, Delgado R. Fortuny A, et al. Among authors: soler a. Prenat Diagn. 1995 Jun;15(6):541-50. doi: 10.1002/pd.1970150607. Prenat Diagn. 1995. PMID: 7544897

5

Rapid fetal karyotype from cystic hygroma and pleural effusions.

Costa D, Borrell A, Margarit E, Carrió A, Soler A, Balmes I, Estivill X, Fortuny A. Costa D, et al. Among authors: soler a. Prenat Diagn. 1995 Feb;15(2):141-8. doi: 10.1002/pd.1970150206. Prenat Diagn. 1995. PMID: 7784365

6

Transcervical chorionic villus sampling beyond 12 weeks of gestation.

Borrell A, Costa D, Delgado RD, Fuster JJ, Soler A, Cararach J, Fortuny A. Borrell A, et al. Among authors: soler a. Ultrasound Obstet Gynecol. 1996 Jun;7(6):416-20. doi: 10.1046/j.1469-0705.1996.07060416.x. Ultrasound Obstet Gynecol. 1996. PMID: 8807757 Free article.

7

Cytogenetic studies in fetal blood.

Costa D, Borrell A, Soler A, Carrió A, Margarit E, Ballesta F, Puerto B, Caballín MR, Fortuny A. Costa D, et al. Among authors: soler a. Fetal Diagn Ther. 1998 May-Jun;13(3):169-75. doi: 10.1159/000020832. Fetal Diagn Ther. 1998. PMID: 9708441

8

Molecular, cytogenetic, and clinical characterisation of six XX males including one prenatal diagnosis.

Margarit E, Soler A, Carrió A, Oliva R, Costa D, Vendrell T, Rosell J, Ballesta F. Margarit E, et al. Among authors: soler a. J Med Genet. 1998 Sep;35(9):727-30. doi: 10.1136/jmg.35.9.727. J Med Genet. 1998. PMID: 9733030 Free PMC article.

9

Trisomy/tetrasomy 21 mosaicism in CVS: interpretation of cytogenetic discrepancies between placental and fetal chromosome complements.

Soler A, Margarit E, Carrió A, Costa D, Queralt R, Ballesta F. Soler A, et al. J Med Genet. 1999 Apr;36(4):333-4. J Med Genet. 1999. PMID: 10227405 Free PMC article.

10

Fetoplacental discrepancy involving structural abnormalities of chromosome 8 detected by prenatal diagnosis.

Soler A, Sánchez A, Carrió A, Badenas C, Milà M, Borrell A. Soler A, et al. Prenat Diagn. 2003 Apr;23(4):319-22. doi: 10.1002/pd.590. Prenat Diagn. 2003. PMID: 12673638

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