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Yayın Arama

Toplam 27840 kayıt

A 46 XXdel X p22 1 22 2 case relevant to its clinical findings
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
Abstracts of the 1th Eurepean Cytogenetics Conference

Short stature and other clinical findings of a case with karyotype 46 XYdel Y q11 2 12 mar
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
Abstracts of the 1th Eurepean Cytogenetics Conference.

Chromosome 2 fragility in 48 XXYY syndrome
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
Second European Cytogenetics Conference

Two siblings Androgen Insensitivity Syndrome with 45 XY t 13q 14q and one is normal 46 XY karyotipes Three case reports
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
Annual Metting of the European Society of Human Genetics

Increased sister chromatide exchange frequency in tyroid cancer patients that treated with I1313 previous results of one case
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
Third European Conference

Molecular and cytogenetic characterisation of a female of hypoplastic external genitalia with a familial Y 21 translocation
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
5.th Euoropean Cytogenetics Conference, Madrid, SPAIN.

The SSCP profiles of mutated homeobox PAX9 gene in orofacial clefts in human
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
5.th Euoropean Cytogenetics Conference,Madrid, SPAIN.

Chromosome 7 duplication in a young girl with congenital heart disease unusual behaviours and low IQ level clinical and cytogenetical characterisation
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Human Genetics conference Amsterdam, The Netherlands

Mutated SSCP profiles of c myc proto oncogene in bladder s papillary urothelial transitional cell neoplasms
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
A molecular approach to cell prolifeCHROMOSOME RESEARCH

Heterozygous deletion of exon 8 in WFS1 gene in two Wolfram Syndrome probands with hearing loss
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
7th European Cytogenetics Conference

The combined effect of K ras proto oncogene and promoter hypermethylation of tumor supressor SFRP2 gene in a case with mucinous anal carcinoma A case report
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
7th European Cytogenetics Conference

Epigenetik alterations and oncogenes mutations in urinary bladder carcinoma
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
7th European Cytogenetics Conference

The crucial role of MDR1 ABCB1 gene polymorphism in abdominal aortic aneurysm A preliminary results of a pilot study
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
7th European Cytogenetics Conference

Tumoral tissue specific promoter hypermethylation of tumor supressor genes SFRp2 p16 DAPK1 HIC and MGMT in a case with non small cell carcinoma A case report
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
7th European Cytogenetics Conference

CRUCIAL ROLE OF PARENTAL MTHFR GENE POLYMORPHISM INVOLVED IN HOMOCYSTEINE METABOLISM IN DOWN SYNDROME
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
IUBMB LIFE

ETERMINATION OF DISTRIBUTION OF COMMON MEFV GENE MUTATIONS IN HEALTHY INDIVIDUALS WHO HAD BEEN EXPOSED TO APPENDECTOMY IN CHILDHOOD AGE
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
IUBMB LIFE

ANGIOTENSIN CONVERTING ENZYME ACE GENE POLYMORPHISM AND BUERGER S DISEASE
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
IUBMB LIFE

Increased T allele frequency in MTHFR C677T gene in thyroid carcinme
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
8th European Cytogenetic Conference

The endemic RTL80V I and RTM204V I YMDD mutation profiles in a case of chronic hepatitis B
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
8th European Cytogenetic Conference

Epigenetic silencing of the tumor supressor HIC1 and SFRP2 genes in prostate carcinomas
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Cytogenetic Conference