Côté GB - Search Results

1

Direct duplication of 8p21.3-->p23.1: a cytogenetic anomaly associated with developmental delay without consistent clinical features.

Fan YS, Siu VM, Jung JH, Farrell SA, Côté GB. Fan YS, et al. Among authors: cote gb. Am J Med Genet. 2001 Oct 15;103(3):231-4. doi: 10.1002/ajmg.1534.abs. Am J Med Genet. 2001. PMID: 11745996

2

Partial trisomy 6p with karyotype 46,XY,der(22), t(6;22)(p22;q13)mat.

Côté GB, Papadakou-Lagoyanni S, Sbyrakis S. Côté GB, et al. J Med Genet. 1978 Dec;15(6):479-81. doi: 10.1136/jmg.15.6.479. J Med Genet. 1978. PMID: 745220 Free PMC article.

3

The effects of severe mixed environmental pollution on human chromosomes.

Katsantoni A, Nakou S, Antoniadou-Koumatou I, Côté GB. Katsantoni A, et al. Among authors: cote gb. J Med Genet. 1986 Oct;23(5):452-5. doi: 10.1136/jmg.23.5.452. J Med Genet. 1986. PMID: 3783622 Free PMC article.

4

New syndrome of trichodermal defect and mental retardation.

Katsantoni A, Papadakou-Lagoyanni S, Micheloyannis J, Côté GB. Katsantoni A, et al. Among authors: cote gb. Am J Med Genet. 1984 Jun;18(2):229-31. doi: 10.1002/ajmg.1320180217. Am J Med Genet. 1984. PMID: 6465198 No abstract available.

5

The cytogenetic and clinical implications of a ring chromosome 2.

Cote GB, Katsantoni A, Deligeorgis D. Cote GB, et al. Ann Genet. 1981;24(4):231-5. Ann Genet. 1981. PMID: 6977305

6

Hypothyroidism and sex chromosomes.

Sarri C, Côté GB, Mengreli C, Lambadaridis I, Pantelakis S. Sarri C, et al. Among authors: cote gb. J Med Genet. 1988 Apr;25(4):247-9. doi: 10.1136/jmg.25.4.247. J Med Genet. 1988. PMID: 3367350 Free PMC article.

7

A gene for hypospadias in a child with presumed tetrasomy 18p.

Côté GB, Petmezaki S, Bastakis N. Côté GB, et al. Am J Med Genet. 1979;4(2):141-6. doi: 10.1002/ajmg.1320040206. Am J Med Genet. 1979. PMID: 293130

8

Beta-thalassaemia: increased chromosomal anomalies in lymphocyte cultures.

Côté GB, Papadakou-Lagoyanni S. Côté GB, et al. J Med Genet. 1979 Feb;16(1):52-5. doi: 10.1136/jmg.16.1.52. J Med Genet. 1979. PMID: 469887 Free PMC article.

9

A cascade of chromosomal aberrations in three generations: a fragile 16q, an extra fragment and a rearranged 20.

Côté GB, Papadakou-Lagoyanni S, Pantelakis S. Côté GB, et al. Ann Genet. 1978 Dec;21(4):209-14. Ann Genet. 1978. PMID: 314256

10

Fryns syndrome without deletion 16q.

Coté GB, Papadakou-Lagoyanni S, Kairis M. Coté GB, et al. Ann Genet. 1980;23(3):171-2. Ann Genet. 1980. PMID: 6968534

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