Gyftodimou J - Search Results

1

A linkage study of the locus for X-linked Charcot-Marie-Tooth disease.

Goonewardena P, Welihinda J, Anvret M, Gyftodimou J, Haegermark A, Iselius L, Lindsten J, Pettersson U. Goonewardena P, et al. Among authors: gyftodimou j. Clin Genet. 1988 Jun;33(6):435-40. doi: 10.1111/j.1399-0004.1988.tb03477.x. Clin Genet. 1988. PMID: 2901924

2

[Retinitis pigmentosa--more families are needed to localize the genes].

Gyftodimou J, Anvret M, Goonewardena P, Pettersson U. Gyftodimou J, et al. Lakartidningen. 1986 Oct 1;83(40):3323, 3326-7. Lakartidningen. 1986. PMID: 3784705 Swedish. No abstract available.

3

Angelman syndrome with uniparental disomy due to paternal meiosis II nondisjunction.

Gyftodimou J, Karadima G, Pandelia E, Vassilopoulos D, Petersen MB. Gyftodimou J, et al. Clin Genet. 1999 Jun;55(6):483-6. doi: 10.1034/j.1399-0004.1999.550615.x. Clin Genet. 1999. PMID: 10450868

4

Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: case report and review of the literature on partial trisomy 17qter.

Sarri C, Gyftodimou J, Avramopoulos D, Grigoriadou M, Pedersen W, Pandelia E, Pangalos C, Abazis D, Kitsos G, Vassilopoulos D, Brøndum-Nielsen K, Petersen MB. Sarri C, et al. Among authors: gyftodimou j. Am J Med Genet. 1997 May 2;70(1):87-94. doi: 10.1002/(sici)1096-8628(19970502)70:1<87::aid-ajmg16>3.0.co;2-t. Am J Med Genet. 1997. PMID: 9129747 Review.

5

Twinning and mitotic crossing-over: some possibilities and their implications.

Côté GB, Gyftodimou J. Côté GB, et al. Among authors: gyftodimou j. Am J Hum Genet. 1991 Jul;49(1):120-30. Am J Hum Genet. 1991. PMID: 2063864 Free PMC article. Review.

6

Molecular and clinical correlation study of Williams-Beuren syndrome: No evidence of molecular factors in the deletion region or imprinting affecting clinical outcome.

Wang MS, Schinzel A, Kotzot D, Balmer D, Casey R, Chodirker BN, Gyftodimou J, Petersen MB, Lopez-Rangel E, Robinson WP. Wang MS, et al. Among authors: gyftodimou j. Am J Med Genet. 1999 Sep 3;86(1):34-43. Am J Med Genet. 1999. PMID: 10440826

7

Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: clinical, cytogenetic and molecular analysis.

Velissariou V, Antoniadi T, Gyftodimou J, Bakou K, Grigoriadou M, Christopoulou S, Hatzipouliou A, Donoghue J, Karatzis P, Katsarou E, Petersen MB. Velissariou V, et al. Among authors: gyftodimou j. Eur J Hum Genet. 2002 Nov;10(11):694-8. doi: 10.1038/sj.ejhg.5200867. Eur J Hum Genet. 2002. PMID: 12404100

8

A report of pure 7p duplication syndrome and review of the literature.

Papadopoulou E, Sifakis S, Sarri C, Gyftodimou J, Liehr T, Mrasek K, Kalmanti M, Petersen MB. Papadopoulou E, et al. Among authors: gyftodimou j. Am J Med Genet A. 2006 Dec 15;140(24):2802-6. doi: 10.1002/ajmg.a.31538. Am J Med Genet A. 2006. PMID: 17103460 Review.

9

Double supernumerary isodicentric chromosomes derived from 15 resulting in partial hexasomy.

Qumsiyeh MB, Rafi SK, Sarri C, Grigoriadou M, Gyftodimou J, Pandelia E, Laskari H, Petersen MB. Qumsiyeh MB, et al. Among authors: gyftodimou j. Am J Med Genet A. 2003 Feb 1;116A(4):356-9. doi: 10.1002/ajmg.a.10050. Am J Med Genet A. 2003. PMID: 12522791

10

A case of partial trisomy of chromosome 8p associated with autism.

Papanikolaou K, Paliokosta E, Gyftodimou J, Kolaitis G, Vgenopoulou S, Sarri C, Tsiantis J. Papanikolaou K, et al. Among authors: gyftodimou j. J Autism Dev Disord. 2006 Jul;36(5):705-9. doi: 10.1007/s10803-006-0104-3. J Autism Dev Disord. 2006. PMID: 16602035

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