N. Laban

发表

Billateral Polycystic Kidneys in a Girl with WAGR Syndrome

J. Crolla, Z. Gucev, V. Tasic, 2011, Indian journal of pediatrics.

Early-onset ocular ochronosis in a girl with alkaptonuria (AKU) and a novel mutation in homogentisate 1,2-dioxygenase (HGD).

Z. Gucev, V. Tasic, A. Zatkova, 2011, Prilozi.

Heterotopic ossifications and Charcot joints: Congenital insensitivity to pain with anhidrosis (CIPA) and a novel NTRK1 gene mutation.

Z. Gucev, V. Tasic, D. Plaseska-Karanfilska, 2019, European journal of medical genetics.

Characteristic Diagnostic Clues of Metatropic Dysplasia: The Lumbothoracic Humpback with Dumbbell Appearance of the Long Bones

Z. Gucev, V. Tasic, D. Plaseska-Karanfilska, 2018, Balkan Journal of Medical Genetics : BJMG.

Emanuel Syndrome (Es): New Case-Report and Review of the Literature/ Емануел Синдром (Es): Презентација На Нов Случај И Преглед На Литературата

Z. Gucev, V. Tasic, D. Danilovski, 2015, Prilozi.

Rare diseases with renal involvement in the Republic of Macedonia.

Z. Gucev, V. Tasic, N. Pop-Jordanova, 2011, Prilozi.

A 4-Year-Old Boy with Beckwith Wiedemann Syndrome (BWS)

Z. Gucev, V. Tasic, C. Bergmann, 2018, Prilozi.

Congenital erythropoietic porphyria with two mutations of the uroporphyrinogen III synthase gene (Cys73Arg, Thr228Met)

Z. Gucev, V. Tasic, N. Pop-Jordanova, 2011, Indian journal of human genetics.

Duplication of The SOX3 Gene in an Sry-negative 46,XX Male with Associated Congenital Anomalies of Kidneys and the Urinary Tract: Case Report and Review of the Literature

Z. Gucev, V. Tasic, S. Sanna-Cherchi, 2019, Balkan journal of medical genetics : BJMG.

Severe Scoliosis, Torticollis and Short Stature in a Woman with Wildervanck Syndrome (WS)/ Изразена Сколиоза, Тортиколис И Низок Раст Кај Жена Со Wildervanck Syndrome (Синдром На Вилдерванк)

Z. Gucev, V. Tasic, M. Polenaković, 2015, Prilozi.

Acute Gallbladder Hydrops and Arthritis: unusual initial manifestations of Wilson's Disease (WD): Case Report.

Z. Gucev, V. Tasic, N. Pop-Jordanova, 2011, Prilozi.

Tissue-specific mosaicism in a patient with Rubinstein-Taybi syndrome and CREBBP exon 1 duplication.

Z. Gucev, V. Tasic, U. Zechner, 2019, Clinical dysmorphology.

Severe digital malformations in a rare variant of fibrodysplasia ossificans progressiva

Z. Gucev, V. Tasic, D. Plaseska-Karanfilska, 2019, American journal of medical genetics. Part A.

IGF1R Gene Alterations in Children Born Small for Gestitional Age (SGA)

Z. Gucev, V. Tasic, J. Kratzsch, 2018, Open access Macedonian journal of medical sciences.

Early-onset ocular ochronosis in a girl with alkaptonuria (AKU) and a novel mutation in homogentisate 1,2-dioxygenase (HGD).

Z. Gucev, D. Danilovski, N. Laban, 2011, Prilozi.