Antiñolo G - Search Results

1

Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression.

Borrego S, Sáez ME, Ruiz A, Gimm O, López-Alonso M, Antiñolo G, Eng C. Borrego S, et al. Among authors: antinolo g. J Med Genet. 1999 Oct;36(10):771-4. doi: 10.1136/jmg.36.10.771. J Med Genet. 1999. PMID: 10528857 Free PMC article.

2

[Translocation T(2;9) in a patient with Philadelphia-negative chronic myeloid leukemia in blast crisis].

Antiñolo G, Borrego S, Martín Noya A, Sánchez J, Fernández JM. Antiñolo G, et al. Sangre (Barc). 1992 Oct;37(5):414-5. Sangre (Barc). 1992. PMID: 1293788 Spanish. No abstract available.

3

Familial spastic paraplegia with neuropathy and poikiloderma. A new syndrome?

Antiñolo G, Nieto M, Borrego S, Sierra J, Rufo M, Siljeström ML. Antiñolo G, et al. Clin Genet. 1992 Jun;41(6):281-4. doi: 10.1111/j.1399-0004.1992.tb03397.x. Clin Genet. 1992. PMID: 1623621

4

[Translocation T (1;15) (Q21;P13) in a male with azoospermia].

Antiñolo G, Borrego S, Fernández Vázquez L, Sánchez J. Antiñolo G, et al. Actas Urol Esp. 1989 Nov-Dec;13(6):465-6. Actas Urol Esp. 1989. PMID: 2618838 Spanish.

5

Molecular and clinical analyses of cystic fibrosis in the south of Spain.

Borrego S, Casals T, Dapena J, Fernández E, Giménez J, Cabeza JC, Sánchez J, Antiñolo G. Borrego S, et al. Among authors: antinolo g. Clin Genet. 1994 Oct;46(4):287-90. doi: 10.1111/j.1399-0004.1994.tb04161.x. Clin Genet. 1994. PMID: 7530610

6

Megalocornea-mental retardation syndrome: an additional case.

Antiñolo G, Rufo M, Borrego S, Morales C. Antiñolo G, et al. Am J Med Genet. 1994 Aug 15;52(2):196-7. doi: 10.1002/ajmg.1320520214. Am J Med Genet. 1994. PMID: 7802008 Review.

7

Identification of a new mutation at codon 171 of rhodopsin gene causing autosomal dominant retinitis pigmentosa.

Antiñolo G, Sánchez B, Borrego S, Rueda T, Chaparro P, Cabeza JC. Antiñolo G, et al. Hum Mol Genet. 1994 Aug;3(8):1421. doi: 10.1093/hmg/3.8.1421. Hum Mol Genet. 1994. PMID: 7987326 No abstract available.

8

Translocation (8;12) in a patient with agnogenic myeloid metaplasia.

Borrego S, Antiñolo G, Martín-Noya A, Parody R. Borrego S, et al. Among authors: antinolo g. Cancer Genet Cytogenet. 1993 Dec;71(2):183-4. doi: 10.1016/0165-4608(93)90030-p. Cancer Genet Cytogenet. 1993. PMID: 8281526 No abstract available.

9

Translocation (14;18) in a patient with common acute lymphoblastic leukemia (FAB l2).

Borrego S, Antiñolo G, Parody R, Jiménez F. Borrego S, et al. Among authors: antinolo g. Cancer Genet Cytogenet. 1993 Feb;65(2):177-8. doi: 10.1016/0165-4608(93)90232-b. Cancer Genet Cytogenet. 1993. PMID: 8453607 No abstract available.

10

Reverse mutation in fragile X syndrome.

Antiñolo G, Borrego S, Cabeza JC, Sánchez R, Sánchez J, Sánchez B. Antiñolo G, et al. Am J Hum Genet. 1996 Jan;58(1):237-9. Am J Hum Genet. 1996. PMID: 8554061 Free PMC article. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

206 results

Search Page

Filters