Pérez C - Search Results

1

Two cases of tetrasomy 9p syndrome with tissue limited mosaicism.

Lloveras E, Pérez C, Solé F, Zamora L, Lladonosa A, Espinet B, Silvestre E, Serra J, Vendrell T, Fernández B, Salido M, Plaja A. Lloveras E, et al. Among authors: perez c. Am J Med Genet A. 2004 Feb 1;124A(4):402-6. doi: 10.1002/ajmg.a.20447. Am J Med Genet A. 2004. PMID: 14735590

2

Bends in human mitotic metaphase chromosomes revisited: 15q11-13 is the most frequent non-random autosomal bend in blood cultures.

Plaja A, Miró R, Fuster C, Perez C, Sarret E, Esteve P, Egozcue J. Plaja A, et al. Among authors: perez c. Am J Med Genet. 2001 Jun 15;101(2):106-13. doi: 10.1002/1096-8628(20010615)101:2<106::aid-ajmg1339>3.0.co;2-z. Am J Med Genet. 2001. PMID: 11391652

3

A female infant with a 46,XX/48,XY, +8, +10 karyotype in prenatal diagnosis: a 'vanishing twin' phenomenon?

Lloveras E, Lecumberri JM, Pérez C, Melero C, Zamora L, Sánchez MA, Solé F, Plaja A. Lloveras E, et al. Among authors: perez c. Prenat Diagn. 2001 Oct;21(10):896-7. doi: 10.1002/pd.174. Prenat Diagn. 2001. PMID: 11746139 No abstract available.

4

Chromosome aneuploidy and cancer: lessons from a chromosomal instability syndrome.

Plaja A, Perez C, Miró R. Plaja A, et al. Among authors: perez c. Cancer Genet Cytogenet. 2001 Dec;131(2):144-5. doi: 10.1016/s0165-4608(01)00501-5. Cancer Genet Cytogenet. 2001. PMID: 11750055 No abstract available.

5

Is the gain of 9p involved in the pathogenesis of polycythemia vera? A purpose of a case.

Zamora L, Lloveras E, Espinet B, Muñoz C, Perez C, Plaja A. Zamora L, et al. Among authors: perez c. Haematologica. 2002 Jan;87(1):ECR05. Haematologica. 2002. PMID: 11801479 No abstract available.

6

Prenatal detection of a paracentric inversion 16(q11.2q13).

Pérez C, Lloveras E, Zamora L, Melero C, Pérez E, Plaja A. Pérez C, et al. Among authors: perez e. Ann Genet. 2002 Jul-Sep;45(3):141-2. doi: 10.1016/s0003-3995(02)01125-5. Ann Genet. 2002. PMID: 12381445

7

Ectopic nucleolus organizer regions in a patient with premature ovarian failure.

Lloveras E, Zamora L, Pérez C, Fuster C, Andreu S, Plaja A. Lloveras E, et al. Among authors: perez c. Fertil Steril. 2006 Oct;86(4):1001.e15-6. doi: 10.1016/j.fertnstert.2006.02.125. Fertil Steril. 2006. PMID: 17027366 Free article.

8

Genomic Chaos (Multiple Copy Number Variations and Structural Reorganization) Detected in Two Prenatal Cases.

Lloveras E, Canellas A, Plaja A, Barranco L, Fernández D, Mendez B, Piqué M, de la Iglesia C, Palau N, Costa M, Herrero M, Yeste D, Auge M, Puig L, Pérez C. Lloveras E, et al. Among authors: perez c. Cytogenet Genome Res. 2021;161(5):236-242. doi: 10.1159/000515653. Epub 2021 Jul 16. Cytogenet Genome Res. 2021. PMID: 34274931

9

A New Case with Corpus Callosum Abnormalities, Microcephaly and Seizures Associated with a 2.3-Mb 1q43-q44 Deletion.

Lloveras E, Canellas A, Barranco L, Alves C, Vila-Real M, Ventura V, Fernández D, Mendez B, Piqué M, Reis-Lima M, de la Iglesia C, Palau N, Costa M, Yeste D, Auge M, Perez C. Lloveras E, et al. Among authors: perez c. Cytogenet Genome Res. 2019;159(3):126-129. doi: 10.1159/000504424. Epub 2019 Dec 13. Cytogenet Genome Res. 2019. PMID: 31830750

10

Tandem Triplication 11p15.5-ICR1 (H19/IGF2) Detected by Microarray and Optical Genome Mapping in a Prenatal Beckwith-Wiedemann Case.

Lloveras E, Pérez C, Mendez B, Martin S, Alves C, Reis-Lima M. Lloveras E, et al. Among authors: perez c. Cytogenet Genome Res. 2023;163(1-2):32-35. doi: 10.1159/000531703. Epub 2023 Jun 27. Cytogenet Genome Res. 2023. PMID: 37369188

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