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Zagradišnik, Boris
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1

Assessing 48 SNPs in Hypertensive Paediatric Patients and Y..:

Močnik, Mirjam ; Zagradišnik, Boris ; Marčun Varda, Nataša
Children.  9 (2022)  8 - p. 1262 , 2022
Link: https://doi.org/10.3390/..
 
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2

Detection of aneuploidy using multiplex ligation–dependent ..:

Zagradišnik, Boris ; Stangler Herodež, Špela ; Erjavec-Škerget, Alenka..
Acta Medico-Biotechnica.  4 (2021)  2 - p. 51-60 , 2021
Link: https://doi.org/10.18690..
 
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3

Identification of genomic copy number variations associated..:

Zagradišnik, Boris ; Krgović, Danijela ; Herodež, Špela Stangler...
Molecular Cytogenetics.  11 (2018)  1 - p. , 2018
Link: https://doi.org/10.1186/..
 
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4

A mosaic form of microphthalmia with linear skin defects:

Prepeluh, Nina ; Korpar, Bojan ; Zagorac, Andreja...
BMC Pediatrics.  18 (2018)  1 - p. , 2018
Link: https://doi.org/10.1186/..
 
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5

Predictive value of paroxysmal EEG abnormalities for future..:

Gradisnik, Peter ; Zagradisnik, Boris ; Palfy, Miroslav..
Brain and Development.  37 (2015)  9 - p. 868-873 , 2015
Link: https://doi.org/10.1016/..
 
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6

An evaluation of SOX2 and hTERC gene amplifications as scre..:

Kokalj Vokač, Nadja ; Čizmarević, Bogdan ; Zagorac, Andreja..
Molecular Cytogenetics.  7 (2014)  1 - p. 5 , 2014
Link: https://doi.org/10.1186/..
 
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7

The association of the JAK2 46/1 haplotype with non-splanch..:

Zerjavic, Katja ; Zagradisnik, Boris ; Lokar, Lidija..
Thrombosis Research.  132 (2013)  2 - p. e86-e93 , 2013
Link: https://doi.org/10.1016/..
 
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8

Deletion of the last exon of SHANK3 gene produces the full ..:

Macedoni-Lukšič, Marta ; Krgović, Danijela ; Zagradišnik, Boris.
Gene.  524 (2013)  2 - p. 386-389 , 2013
Link: https://doi.org/10.1016/..
 
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9

Strong intra- and inter-continental differentiation reveale..:

Cruciani, Fulvio ; Trombetta, Beniamino ; Antonelli, Cheyenne...
Forensic Science International: Genetics.  5 (2011)  3 - p. e49-e52 , 2011
Link: https://doi.org/10.1016/..
 
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10

Polymorphisms in four candidate genes in young patients wit..:

Marčun Varda, Nataša ; Zagradišnik, Boris ; Stangler Herodež, Špela..
Acta Paediatrica.  95 (2006)  3 - p. 353-358 , 2006
Link: https://doi.org/10.1111/..
 
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11

Polymorphisms in four candidate genes in young patients wit..:

Marčun Varda, Nataša ; Zagradišnik, Boris ; Stangler Herodež, Špela..
Acta Paediatrica.  95 (2006)  3 - p. 353-358 , 2006
Link: https://doi.org/10.1080/..
 
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12

A case of Shwachman‐Diamond syndrome in a male neonate:

Todorovič‐Guid, Mirjana ; Krajnc, Olga ; Marcun Varda, Natasa...
Acta Paediatrica.  95 (2006)  7 - p. 892-893 , 2006
Link: https://doi.org/10.1111/..
 
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13

A case of Shwachman-Diamond syndrome in a male neonate:

Todorovič-Guid, Mirjana ; Krajnc, Olga ; Marcun Varda, Natasa...
Acta Paediatrica.  95 (2006)  7 - p. 892-893 , 2006
Link: https://doi.org/10.1080/..
 
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14

Eighteen-year follow-up of a patient with partial hypoxanth..:

Gregorič, Alojz ; Rabelink, Gwenda M. ; Vokač, Nadja Kokalj..
Pediatric Nephrology.  20 (2005)  9 - p. 1346-1348 , 2005
Link: https://doi.org/10.1007/..
 
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15

Subterminal deletion/duplication event in an affected male ..:

Kokalj-Vokac, Nadja ; Marcun-Varda, Natasa ; Zagorac, Andreja...
European Journal of Pediatrics.  , 2004
Link: https://doi.org/10.1007/..
 
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