vol 21
Number VOL. 21(2), 2018
12/19/2018
Front cover page: Golden funeral glove, 5th century BC, Lychnidos, Ohrid Museum

Back cover page: Golden anthropomorphous earrings, 3rd century BC, Lychnidos, Ohrid Museum
Cover design: Bitrakova-Grozdanova V, Skopje
THE FREQUENCY OF EGFR AND KRAS MUTATIONS IN THE TURKISH POPULATION WITH NON-SMALL CELL LUNG CANCER AND THEIR RESPONSE TO ERLOTINIB THERAPY
Demiray A, Yaren A, Karagenç N, Bir F, Demiray AG, Karagür ER, Tokgün O, Elmas L, Akça H, https://orcid.org/0000-0002-3343-0184.
page: 21
PRENATAL DIAGNOSIS OF A NEW CASE: DE NOVO BALANCED NON-ROBERTSONIAN TRANSLOCATION INVOLVING t(15;22)(p11.2;q11.2)
Atli Eİ, Gurkan H, Atli E, Tozkir H, Varol GF, İnan C
page: 69
A NOVEL DE NOVO PARACENTRIC INVERSION [inv(20)(q13.1q13.3)] ACCOMPANIED BY AN 11q14.3-q21 MICRODELETION IN A PEDIATRIC PATIENT WITH AN INTELLECTUAL DISABILITY
Zachaki S, Kouvidi E, Mitrakos A, Lazaros L, Pantou A, Mavrou A, Tzetis M, Manola KN
page: 63
RARE CASE OF A HETEROZYGOUS MICRODELETION 9q21.11-q21.2: CLINICAL AND GENETIC CHARACTERISTICS
Ivanov HY, Stoyanova V, Ivanov I, Linev A, Vazharova R, Ivanov S, Balabanski L, Toncheva D
page: 59
A NOVEL MUTATION IN A NEWBORN BABY LEADING TO GLYCOGEN STORAGE DISEASE TYPE IA
Dorum S, Gorukmez O
page: 55
THE ROLE OF NEXT GENERATION SEQUENCING IN THE DIFFERENTIAL DIAGNOSIS OF CAROLIíS SYNDROME
Smolović B, Muhović D, Hodžić A, Bergant G, Peterlin B
page: 49
NEXT GENERATION SEQUENCING IDENTIFIED A NOVEL MULTI EXON DELETION OF THE NF1 GENE IN A CHINESE PEDIGREE WITH NEUROFIBROMATOSIS TYPE 1
Yang J, An J-X, Liu X-L, Wang Z-Q, Xie G-M, Yang X-L, Xu S-J, Feng F, Ni Y -- Jie Yang and Jinxia An contributed equally to this study.
page: 45
MYOTONIC DYSTROPHY-2: UNUSUAL PHENOTYPE DUE TO A SMALL CCTG-EXPANSION
Finsterer J, Stöllberger C, Reining-Festa A, Loewe-Grgurin M, Gencik M
page: 39
EPIGENETIC SIGNATURE OF CHRONIC MATERNAL STRESS LOAD DURING PREGNANCY MIGHT BE A POTENTIAL BIOMARKER FOR SPONTANEOUS PRETERM BIRTH
Rogac M, Peterlin B
page: 27
DETERMINING SPECIFIC THYROID TRANSCRIPTS IN PERIPHERAL BLOOD: A SINGLE CENTER STUDY EXPERIENCE
Makazlieva T, Eftimov A, Vaskova O, Tripunoski T, Miladinova D, Risteski S, Jovanovic H, Jakovski Z Tanja Makazlieva and Aleksandar Eftimov contributed equally to this study and are considered first coauthors.
page: 13
INVESTIGATION OF CIRCULATING SERUM microRNA-328-3p AND microRNA-3135a EXPRESSION AS PROMISING NOVEL BIOMARKERS FOR AUTISM SPECTRUM DISORDER
Popov NT, Minchev DS, Naydenov MM, Minkov IN, Vachev TI
page: 5
A FAMILIAL CASE REPORT OF A 13;22 CHROMOSOMAL TRANSLOCATION WITH RECURRENT INTRACYTOPLASMIC SPERM INJECTION FAILURE
Verma S, Shah R, Bhat A, Bhat GR, Dada R, Kumar R,
page: 73
CHARACTERISTIC DIAGNOSTIC CLUES OF METATROPIC DYSPLASIA: THE LUMBOTHORACIC HUMPBACK WITH DUMBBELL APPEARANCE OF THE LONG BONES
Gucev Z, Kalcev G, Laban N, Bozinovski Z, Popovski N, Saveski A, Daskalov B, Plaseska-Karanfilska D, Tasic V
page: 35



Number 21
VOL. 21(2), 2018
Number 21
VOL. 21 (1), 2018
Number 21
VOL. 21, 2018 Accepted articles
Number 21
VOL. 21, 2018 Supplement
Number 20
VOL. 20 (2), 2017
Number 20
VOL. 20 (1), 2017
Number 19
VOL. 19 (2), 2016
Number 19
VOL. 19 (1), 2016
Number 18
VOL. 18 (2), 2015
Number 18
VOL. 18 (1), 2015
Number 17
VOL. 17 (2), 2014
Number 17
VOL. 17 (1), 2014
Number 16
VOL. 16 (2), 2013
Number 16
VOL. 16 (1), 2013
Number 15
VOL. 15 (2), 2012
Number 15
VOL. 15, 2012 Supplement
Number 15
Vol. 15 (1), 2012
Number 14
14 - Vol. 14 (2), 2011
Number 14
The 9th Balkan Congress of Medical Genetics
Number 14
14 - Vol. 14 (1), 2011
Number 13
Vol. 13 (2), 2010
Number 13
Vol.13 (1), 2010
Number 12
Vol.12 (2), 2009
Number 12
Vol.12 (1), 2009
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Vol.11 (2),2008
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Vol.11 (1),2008
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10 (1),2007
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1&2, 2006
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3&4, 2006
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3&4, 2001
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1&2, 2001
Number 3
Vol.3 (3), 2000
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Vol.2 (3), 1999
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Vol.1 (3), 1998
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Vol.3(2), 2000
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Vol.1 (2), 1998
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Vol.2 (2), 1999
Number 1
Vol.3 (1), 2000
Number 1
Vol.2 (1), 1999
Number 1
Vol.1 (1), 1998

 

 


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