Sanz R - Search Results

1

Chromosomal mosaicism for isochromosome 11q confined to CVS direct preparations.

Sanz R, Lorda-Sanchez I, Fernández-Moya JM, Cifuentes-Sulzberger S, Rodríguez de Alba M, Gonzalez-Gonzalez MC, Ibañez MA, Robledo M, Ayuso C, Ramos C. Sanz R, et al. Fetal Diagn Ther. 2001 Mar-Apr;16(2):95-7. doi: 10.1159/000053888. Fetal Diagn Ther. 2001. PMID: 11173955

2

Prenatal diagnosis on fetal cells obtained from maternal peripheral blood: report of 66 cases.

Rodríguez De Alba M, Palomino P, Jurado A, Sanz R, Ibañez MA, Fernández-Moya JM, Ayuso C, Díaz-Recasens J, Lahoz C, Ramos C. Rodríguez De Alba M, et al. Among authors: sanz r. Prenat Diagn. 1999 Oct;19(10):934-40. doi: 10.1002/(sici)1097-0223(199910)19:10<934::aid-pd675>3.0.co;2-p. Prenat Diagn. 1999. PMID: 10521819 Clinical Trial.

3

Segregation of digital number with partial monosomy or trisomy of 13q in familial 5;13 translocation.

Rodríguez de Alba M, Sanz R, Lorda-Sanchez I, Fernández-Moya JM, Ayuso C, Díaz-Recasens J, Ramos C. Rodríguez de Alba M, et al. Among authors: sanz r. Prenat Diagn. 1999 Sep;19(9):884-6. doi: 10.1002/(sici)1097-0223(199909)19:9<884::aid-pd655>3.0.co;2-w. Prenat Diagn. 1999. PMID: 10521852

4

Rapid identification of a small dicentric supernumerary marker derived from chromosome 16 with a modified FISH technique on amniotic fluid.

Sanz R, Anabitarte MA, Querejeta ME, Lorda-Sanchez I, Ibañez MA, Rodríguez de Alba MR, Ayuso C, Ramos C. Sanz R, et al. Prenat Diagn. 2000 Jan;20(1):63-5. doi: 10.1002/(sici)1097-0223(200001)20:1<63::aid-pd741>3.0.co;2-w. Prenat Diagn. 2000. PMID: 10701855

5

Sonographic, cytogenetic and DNA analysis in four 69,XXX fetuses diagnosed in the second trimester.

Fernández-Moya JM, Sanz R, Rodríguez De Alba M, Ibañez MA, Ayuso C, Díaz-Recasens J, Robledo M, Ramos C. Fernández-Moya JM, et al. Among authors: sanz r. Fetal Diagn Ther. 2000 Mar-Apr;15(2):97-101. doi: 10.1159/000020984. Fetal Diagn Ther. 2000. PMID: 10720874

6

Prenatal diagnosis on fetal cells from maternal blood: practical comparative evaluation of the first and second trimesters.

Rodríguez de Alba M, Palomino P, González-González C, Lorda-Sanchez I, Ibañez MA, Sanz R, Fernández-Moya JM, Ayuso C, Díaz-Recasens J, Ramos C. Rodríguez de Alba M, et al. Among authors: sanz r. Prenat Diagn. 2001 Mar;21(3):165-70. doi: 10.1002/1097-0223(200103)21:3<165::aid-pd29>3.0.co;2-f. Prenat Diagn. 2001. PMID: 11260601

7

Choroideremia, sensorineural deafness, and primary ovarian failure in a woman with a balanced X-4 translocation.

Lorda-Sanchez IJ, Ibañez AJ, Sanz RJ, Trujillo MJ, Anabitarte ME, Querejeta ME, Rodriguez de Alba M, Gimenez A, Infantes F, Ramos C, Garcia-Sandoval B, Ayuso C. Lorda-Sanchez IJ, et al. Among authors: sanz rj. Ophthalmic Genet. 2000 Sep;21(3):185-9. Ophthalmic Genet. 2000. PMID: 11035551

8

[A clinical, cytogenetic and molecular study of 10 patients with the Prader-Willi syndrome].

Barabash A, Robledo M, Sanz R, Renedo M, Ramos C, Ayuso C, Benítez J. Barabash A, et al. Among authors: sanz r. Med Clin (Barc). 1997 Mar 1;108(8):304-6. Med Clin (Barc). 1997. PMID: 9121208 Spanish.

9

Antenatal diagnosis and management of a ranula.

Fernandez Moya JM, Cifuentes Sulzberger S, Díaz Recaséns J, Ramos C, Sanz R, Perez Tejerizo G. Fernandez Moya JM, et al. Among authors: sanz r. Ultrasound Obstet Gynecol. 1998 Feb;11(2):147-8. doi: 10.1046/j.1469-0705.1998.11020147.x. Ultrasound Obstet Gynecol. 1998. PMID: 9549845 Free article.

10

Assignment of the calcium-binding mitochondrial carrier Aralar1 gene (SLC25A12) to human chromosome band 2q31 by in situ hybridization.

Sanz R, del Arco A, Ayuso C, Ramos C, Satrústegui J. Sanz R, et al. Cytogenet Cell Genet. 2000;89(3-4):143-4. doi: 10.1159/000015595. Cytogenet Cell Genet. 2000. PMID: 10965105 No abstract available.

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