M. Mihalatos

发表

A change in the last base of BRCA1 exon 23, 5586G-->A, results in abnormal RNA splicing.

Athens, D. Yannoukakos, E. Efstathiou, 2002, Cancer genetics and cytogenetics.

Germ line BRCA1 & BRCA2 mutations in Greek breast/ovarian cancer families: 5382insC is the most frequent mutation observed.

D. Yannoukakos, N. Haites, A. Schofield, 2002, Cancer letters.

X-linked adrenoleukodystrophy: are signs of hypogonadism always due to testicular failure?

H. Michelakakis, S. Tsagarakis, M. Mihalatos, 2014, Hormones.

Characterization of a novel large deletion and single point mutations in the BRCA1 gene in a Greek cohort of families with suspected hereditary breast cancer

K. Kyriacou, D. Yannoukakos, A. Hadjisavvas, 2004, BMC Cancer.

Rare mutations predisposing to familial adenomatous polyposis in Greek FAP patients

N. Agnantis, G. Fountzilas, A. Apessos, 2005, BMC Cancer.

A modified mutagenic PCR-RFLP method for K-ras codon 12 and 13 mutations detection in NSCLC patients.

K. Anagnostopoulou, P. Kosmidis, M. Mihalatos, 2001, Molecular and cellular probes.

Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report

T. Liehr, M. Petersen, G. Kitsos, 2008, Molecular Cytogenetics.

Novel mutations of the APC gene in familial adenomatous polyposis in Greek patients.

D. Yannoukakos, N. Agnantis, G. Fountzilas, 2003, Cancer genetics and cytogenetics.

hMSH2 is the most commonly mutated MMR gene in a cohort of Greek HNPCC patients

N. Agnantis, G. Fountzilas, A. Apessos, 2005, British Journal of Cancer.

Heterogeneous molecular mechanisms underlie attenuated familial adenomatous polyposis

S. Bione, T. Venesio, G. Ranzani, 2007, Genetics in Medicine.

Incidence of Mycobacterium tuberculosis in Greece in a variety of clinical specimens using PCR assay for the IS6110 and mpt40 genomic loci

G. Nasioulas, N. Vakalis, M. Mihalatos, 2003 .

Prenatal diagnosis of a fetus with 7q11.23 deletion detected by multiplex ligation‐dependent probe amplification (MLPA) screening

E. Anastasiadou, H. Kontos, S. Orrù, 2008, Prenatal diagnosis.