Prieto F - Search Results

1

Two reciprocal translocations t(9p+;13q-) and t(13q-;21q+): a study of the families.

Prieto F, Badia L, Asensi F, Roques V. Prieto F, et al. Hum Genet. 1980;54(1):7-11. doi: 10.1007/BF00279042. Hum Genet. 1980. PMID: 7390483

2

A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation.

Martínez-Garay I, Tomás M, Oltra S, Ramser J, Moltó MD, Prieto F, Meindl A, Kutsche K, Martínez F. Martínez-Garay I, et al. Among authors: prieto f. Eur J Hum Genet. 2007 Jan;15(1):29-34. doi: 10.1038/sj.ejhg.5201717. Epub 2006 Oct 11. Eur J Hum Genet. 2007. PMID: 17033686

3

Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndrome.

Bartsch O, König U, Petersen MB, Poulsen H, Mikkelsen M, Palau F, Prieto F, Schwinger E. Bartsch O, et al. Among authors: prieto f. Hum Genet. 1993 Sep;92(2):127-32. doi: 10.1007/BF00219679. Hum Genet. 1993. PMID: 8370577

4

Heart-hand syndrome. III. A new syndrome in three generations.

Ruiz de la Fuente S, Prieto F. Ruiz de la Fuente S, et al. Among authors: prieto f. Hum Genet. 1980;55(1):43-7. doi: 10.1007/BF00329125. Hum Genet. 1980. PMID: 7450756

5

An autosomal dominant retinitis pigmentosa family with close linkage to D7S480 on 7q.

Millán JM, Martínez F, Vilela C, Beneyto M, Prieto F, Nájera C. Millán JM, et al. Among authors: prieto f. Hum Genet. 1995 Aug;96(2):216-8. doi: 10.1007/BF00207382. Hum Genet. 1995. PMID: 7635473

6

Adjacent 2 translocation involving 13q and 21q.

Prieto F, Badia L. Prieto F, et al. J Med Genet. 1983 Apr;20(2):155. doi: 10.1136/jmg.20.2.155. J Med Genet. 1983. PMID: 6842558 Free PMC article. No abstract available.

7

Translocations involving chromosomes #3 and #12: hematologic diseases associated with abnormalities of these chromosomes.

Sandberg AA, Hecht BK, Ondreyco SM, Prieto F, Hecht F. Sandberg AA, et al. Among authors: prieto f. Cancer Genet Cytogenet. 1982 Sep;7(1):1-17. doi: 10.1016/0165-4608(82)90103-0. Cancer Genet Cytogenet. 1982. PMID: 6754070 Review.

8

Pericentric inversions of chromosome 12 in two families.

Prieto F, Badía L, Asensi F, Moya A, Figuera MJ. Prieto F, et al. Hum Genet. 1981;57(2):131-3. doi: 10.1007/BF00282007. Hum Genet. 1981. PMID: 6453076

9

Is G banding sufficient for the localization of breakpoints in translocations? A comment on the paper: A case of (13q;18q) translocation with proximal 13q monosomy. By Y.Suzuki, K. Ono, S. Oka, T. Matsubara, M. Arima, and Y. Nakagome. Hum. Genet. 38, 337-341 (1977).

Prieto F, Badia L, Asensi F. Prieto F, et al. Hum Genet. 1979 Apr 5;47(3):343-4. doi: 10.1007/BF00321028. Hum Genet. 1979. PMID: 457122 No abstract available.

10

10p- syndrome associated with multiple chromosomal abnormalities.

Prieto F, Badia L, Moreno JA, Barbero P, Asensi F. Prieto F, et al. Hum Genet. 1978 Dec 18;45(2):229-35. doi: 10.1007/BF00286969. Hum Genet. 1978. PMID: 738725

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