Oculo-auriculo-vertebral (Goldenhar) spectrum associated with pericentric inversion 9: coincidental findings or etiologic factor?

M Stanojević , B Koprcina , F Stipoljev , A Kurjak
Journal of Craniofacial Genetics and Developmental Biology 20 ( 3) 150 -154

33
2000
Familial pericentric inversion of chromosome 4: inv(4)(p16.1q12)

F Stipoljev , M Stanojevic , A Kurjak
Clinical Genetics 61 ( 5) 386 -388

1
2002
Partial monosomy 4q and partial trisomy 13q: Phenotype and molecular mapping of the breakpoints

J Wagner , S Dorner , F Stipoljev , I Skrlec
Seventh European Cytogenetics Conference S32 -S32

3
2009
Fetal endocardial fibroelastosis and severe aortic ste nosis

U Marton , M Kos , F Stipoljev , V Latin
Gynecol Perinatol 6 57 -8

2
1997
Fertilization failures: the role of chromosomal aberration and expression of zona pellucida proteins

S Vujisic-Zivkovic , F Stipoljev , S Zidovec , K Branovic
Periodicum Biologorum 102 ( 4) 385 -390

2000
Citogenetsko istraživanje kromosomskih varijanti i abnormalnosti u 125 parova s učestalim spontanim pobačajima.

F Stipoljev , Milan Kos , Berivoj Mišković , Višnja Latin
Gynaecologia et perinatologia 7 ( 3) 105 -108

1998
Noviji napredak u perinatalnom razdoblju

A Kurjak , F Stipoljev , M Gregov , S Vujisić
Medicina 33 ( 1-4) 135 -9

1997
Ultrazvuk i nasljedne bolesti

F Stipoljev , A Kurjak
Kurjak A et al. Ultrazvuk u ginekologiji i porodništvu. Zagreb: Art studio Azinović

Prenatalna dijagnostika

A Kurjak , S Kupešić , F Stipoljev
Polšek D, Pavelić K, eds. Društveni značaj genske tehnologije. Zagreb: Insitut društvenih znanosti Ivo Pilar

Biochemical screening of fetal aneuploidies and neural tube defects by" double-test

D Tislaric-Medenjak , V Kosec , I Tonkovic-Durisevic , I Zec
Croatia: a 10 957 -962

5
Rapid CFTR mutation detetction using kingfisher, lightcycler and line-probe technologies: implications for prenatal diagnosis

Jasminka Sertić , Davor Begović , F Stipoljev , M Kos
international symposium for cystic fibrosis 12 -12

2002
Amelanotic spindle-cell melanoma metastatic to the breast-case report

I Fabijanić , I Kardum-Skelin , D Šušterčić , V Vidjak
32nd European congress of cytology

2006
Phenotypic features in a patient with 1p36 deletion syndrome

F Stipoljev , A Vicic , R Gjergja-Juraski
EUROPEAN JOURNAL OF HUMAN GENETICS 28 ( SUPPL 1) 901 -902

2020
Uloga bronhoskopije u dijagnostici SARS-CoV-2 infekcije-iskustvo jednog centra

A Koprivanac , M Miličević , E Galić , N Marić
11. kongres Hrvatskog torakalnog društva–TORAKS 2021 s međunarodnim sudjelovanjem u postupku objav -u postupku objav

2021
Recurrent triploidy of maternal origin

F Stipoljev , A Vicic , T Hafner , I Drmic Hoffman
CHROMOSOME RESEARCH 17 215 -215

2009
Prenatal diagnosis of double trisomy: Down and Klinefelter syndrome (48, XXY,+ 21)

A Vicic , T Hafner , F Stipoljev
CHROMOSOME RESEARCH 17 214 -215

2009
Complete hydatiform mole with coexisting live newborn in twin gestation

D Jandrić , G Stanić , F Stipoljev , B Mišković
Acta clinica Croatica 46 ( 2) 220 -221

2007
Prenatal detection of a rare population variant 15p

F Stipoljev , R Lasan-Trcic
CHROMOSOME RESEARCH 15 244 -245

2007
1999
Hypophosphatasia: Phenotypic Variability and Possible Croatian Origin of the c.1402G>A Mutation of TNSALP Gene

Ksenija Fumić , Vladimir Sarnavka , Danijela Petković Ramadža , Kristina Potočki
Collegium Antropologicum 33 ( 4) 1255 -1260

5
2009