Fortuny 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. 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. Among authors: fortuny a. Prenat Diagn. 1993 Feb;13(2):137-41. doi: 10.1002/pd.1970130209. Prenat Diagn. 1993. PMID: 8464833

3

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. Prenat Diagn. 1995 Jun;15(6):541-50. doi: 10.1002/pd.1970150607. Prenat Diagn. 1995. PMID: 7544897

4

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: fortuny a. Prenat Diagn. 1995 Feb;15(2):141-8. doi: 10.1002/pd.1970150206. Prenat Diagn. 1995. PMID: 7784365

5

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: fortuny 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.

6

Brachycephaly is ineffective for detection of Down syndrome in early midtrimester fetuses.

Borrell A, Costa D, Martinez JM, Puerto B, Carrio A, Ojuel J, Fortuny A. Borrell A, et al. Among authors: fortuny a. Early Hum Dev. 1997 Jan 3;47(1):57-61. doi: 10.1016/s0378-3782(96)01784-7. Early Hum Dev. 1997. PMID: 9118829

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: fortuny a. Fetal Diagn Ther. 1998 May-Jun;13(3):169-75. doi: 10.1159/000020832. Fetal Diagn Ther. 1998. PMID: 9708441

8

Pericentric X chromosome in a family.

Soler A, Salami C, Balmes I, Carrio A, Tejada I, Farguell T, Cols N, Cararach J, Fortuny A. Soler A, et al. Among authors: fortuny a. Clin Genet. 1981 Sep;20(3):234-5. doi: 10.1111/j.1399-0004.1981.tb01836.x. Clin Genet. 1981. PMID: 7307323 No abstract available.

9

Natural evolution of nuchal thickness in trisomy-21 fetuses.

Borrell A, Costa D, Martinez JM, Farré MT, Cararach J, Fortuny A. Borrell A, et al. Among authors: fortuny a. Obstet Gynecol. 1998 Jan;91(1):78-81. doi: 10.1016/s0029-7844(97)00576-0. Obstet Gynecol. 1998. PMID: 9464725

10

Ultrasound diagnostic features of twin reversed arterial perfusion sequence.

Borrell A, Pesarrodona A, Puerto B, Deulofeu P, Fuster JJ, Fortuny A. Borrell A, et al. Among authors: fortuny a. Prenat Diagn. 1990 Jul;10(7):443-8. doi: 10.1002/pd.1970100706. Prenat Diagn. 1990. PMID: 2235904

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