Correa-Cerro LS - Search Results

1

Zimmermann-Laband syndrome: further clinical delineation.

Dávalos IP, García-Cruz D, García-Cruz MO, Ramírez-Dueñas ML, Solis-Cámara P, Correa-Cerro LS, Perez-Rulfo D, Sánchez-Corona J. Dávalos IP, et al. Among authors: correa cerro ls. Genet Couns. 2005;16(3):283-90. Genet Couns. 2005. PMID: 16261693

2

Hereditary multiple benign cystic epithelioma (multiple trichoepithelioma) with onset at early age.

Correa-Cerro LS, García-Cruz D, Sarralde A, Morales-Peralta E, González-Mendoza A, Sánchez-Corona J. Correa-Cerro LS, et al. Genet Couns. 1997;8(2):83-6. Genet Couns. 1997. PMID: 9219004

3

De novo duplication xq22-q23 in a girl with short stature and gonadal dysgenesis.

Correa-Cerro L, Garcia-Cruz D, Ruiz MX, Sanchez-Corona J. Correa-Cerro L, et al. Ann Genet. 1999;42(1):41-4. Ann Genet. 1999. PMID: 10214506 Review.

4

Interstitial deletion 6q16.2q22.2 in a child with ectrodactyly.

Correa-Cerro L, Garcíaz-Cruz D, Díaz-Castaños L, Figuera LE, Sanchez-Corona J. Correa-Cerro L, et al. Ann Genet. 1996;39(2):105-9. Ann Genet. 1996. PMID: 8766142

5

Functional Xp disomy and hypomelanosis of Ito.

Rivera H, Correa-Cerro LS, Robinson DO, Crolla JA. Rivera H, et al. Arch Med Res. 2000 Jan-Feb;31(1):88-92. doi: 10.1016/s0188-4409(99)00081-8. Arch Med Res. 2000. PMID: 10767487

6

Functional Xp disomy and de novo t(X;13)(q10;q10) in a girl with hypomelanosis of Ito.

Correa-Cerro LS, Rivera H, Vasquez AI. Correa-Cerro LS, et al. J Med Genet. 1997 Feb;34(2):161-3. doi: 10.1136/jmg.34.2.161. J Med Genet. 1997. PMID: 9039996 Free PMC article.

7

The gene for branchio-oculo-facial syndrome does not colocalize to the EYA1-4 genes.

Correa-Cerro LS, Kennerknecht I, Just W, Vogel W, Müller D. Correa-Cerro LS, et al. J Med Genet. 2000 Aug;37(8):620-3. doi: 10.1136/jmg.37.8.620. J Med Genet. 2000. PMID: 10991692 Free PMC article. No abstract available.

8

Sex determination in Ellobius lutescens: the story of an enigma.

Vogel W, Jainta S, Rau W, Geerkens C, Baumstark A, Correa-Cerro LS, Ebenhoch C, Just W. Vogel W, et al. Cytogenet Cell Genet. 1998;80(1-4):214-21. doi: 10.1159/000014983. Cytogenet Cell Genet. 1998. PMID: 9678361

9

(CAG)nCAA and GGN repeats in the human androgen receptor gene are not associated with prostate cancer in a French-German population.

Correa-Cerro L, Wöhr G, Häussler J, Berthon P, Drelon E, Mangin P, Fournier G, Cussenot O, Kraus P, Just W, Paiss T, Cantú JM, Vogel W. Correa-Cerro L, et al. Eur J Hum Genet. 1999 Apr;7(3):357-62. doi: 10.1038/sj.ejhg.5200298. Eur J Hum Genet. 1999. PMID: 10234512

10

Vitamin D receptor polymorphisms as markers in prostate cancer.

Correa-Cerro L, Berthon P, Häussler J, Bochum S, Drelon E, Mangin P, Fournier G, Paiss T, Cussenot O, Vogel W. Correa-Cerro L, et al. Hum Genet. 1999 Sep;105(3):281-7. doi: 10.1007/s004390051102. Hum Genet. 1999. PMID: 10987658

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