Publications by authors named "Nevenka Laban"

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Heterotopic ossifications and Charcot joints: Congenital insensitivity to pain with anhidrosis (CIPA) and a novel NTRK1 gene mutation.
Zoran Gucev, Velibor Tasic, Ivona Bogevska, Nevenka Laban, Alek Saveski

Eur J Med Genet· January 2020

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Tissue-specific mosaicism in a patient with Rubinstein-Taybi syndrome and CREBBP exon 1 duplication.
Zoran S Gucev, Velibor B Tasic, Aleksandar Saveski, Momir H Polenakovic, Nevenka B Laban

Clin Dysmorphol· July 2019

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Severe digital malformations in a rare variant of fibrodysplasia ossificans progressiva.
Zoran Gucev, Velibor Tasic, Dijana Plaseska-Karanfilska, Marija Dimishkovska, Nevenka Laban

Am J Med Genet A· July 2019

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A 4-Year-Old Boy with Beckwith Wiedemann Syndrome (BWS).
Aleksandra Janchevska, Velibor Tasic, Nevenka Laban, Momir Polenakovic, Zoran Gucev

Pril (Makedon Akad Nauk Umet Odd Med Nauki)· December 2018

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Gene Alterations in Children Born Small for Gestitional Age (SGA).
Aleksandra Janchevska, Marina Krstevska-Konstantinova, Heike Pfäffle, Marina Schlicke, Nevenka Laban

Open Access Maced J Med Sci· November 2018

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LHX4 Gene Alterations: Patient Report and Review of the Literature.
Zoran Gucev, Velibor Tasic, Dijana Plaseska-Karanfilska, Marina Krstevska Konstantinova, Ana Stamatova, Nevenka Laban

Pediatr Endocrinol Rev· June 2016

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Billateral polycystic kidneys in a girl with WAGR syndrome.
Zoran Gucev, Olivera Muratovska, Nevenka Laban, Lence Misevska, Aleksandra Jancevska

Indian J Pediatr· October 2011

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Congenital erythropoietic porphyria with two mutations of the uroporphyrinogen III synthase gene (Cys73Arg, Thr228Met).
Zoran Gucev, Nevenka Slavevska, Velibor Tasic, Nevenka Laban, Nada Pop-Jordanova

Indian J Hum Genet· May 2011

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