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Incompletely Penetrant PKD1 Alleles Mimic the Renal Manifestations of ARPKD

Journal of the American Society of Nephrology, 2010-07, Vol.21 (7), p.1097-1102

2010

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Novel missense mutations in the glycine receptor β subunit gene ( GLRB ) in startle disease

Neurobiology of disease, 2013-04, Vol.52, p.137-149

2013

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Mutations in SPINT2 Cause a Syndromic Form of Congenital Sodium Diarrhea

American journal of human genetics, 2009-02, Vol.84 (2), p.188-196

2009

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Identification of the gene responsible for Best macular dystrophy

Nature genetics, 1998-07, Vol.19 (3), p.241-247

1998

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The first arrival of the Chinese sand roach Polyphaga cf. plancyi (Blattodea: Corydiidae) in Europe

Travaux du Muséum national d'histoire naturelle "Grigore Antipa", 2022, Vol.65 (2), p.163-172

2022

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The first confirmed record of Mediterranean mantis, Iris oratoria (Mantodea: Eremiaphilidae) in Montenegro

Travaux du Muséum national d'histoire naturelle "Grigore Antipa", 2021-12, Vol.64 (2), p.97-101

2021

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Functional analysis of the novel TBX5 c.1333delC mutation resulting in an extended TBX5 protein

BMC medical genetics, 2008-10, Vol.9 (1), p.88-88

2008

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Distribution of genus Libelloides Schaeffer, 1766 (Neuroptera: Ascalaphidae) in Serbia with the help of citizen science

Kragujevac Journal of Science, 2022, Vol.2022 (44), p.215-218

2022

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A new greenhouse invader: the first report of the alien ring-legged earwig, Euborellia annulipes (Dermaptera, Anisolabididae) in Serbia, with the first checklist of earwigs of the country

Travaux du Muséum national d'histoire naturelle "Grigore Antipa", 2022, Vol.65 (2), p.27-38

2022

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Six new hoverfly species (Diptera: Syrphidae) in the fauna of Serbia

Kragujevac Journal of Science, 2021, Vol.2021 (43), p.149-155

2021

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New records and distribution of species from genus Arctophila schiner, 1860 (Diptera: Syrphidae: Eristalinae) in Serbia

Kragujevac Journal of Science, 2020, Vol.2020 (42), p.151-160

2020

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The first record of the wharf borer Nacerdes melanura (Linnaeus, 1758) (Coleoptera: Oedemeridae) in Serbia

Kragujevac Journal of Science, 2024, Vol.46 (1), p.175-178

2024

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A case report of two male siblings with autism and duplication of Xq13–q21, a region including three genes predisposing for autism

European child & adolescent psychiatry, 2014-05, Vol.23 (5), p.329-336

2014

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Functional analysis of the novel TBX5 c. 1333delC mutation resulting in an extended TBX5 protein

BMC medical genetics, 2008-10, Vol.9

2008

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First record of the genus Xeropicta Monterosato, 1892 (Gastropoda: Eupulmonata: Geomitridae) in Serbia

Folia malacologica, 2022-03, Vol.30 (1), p.47-53

2022

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New records of allochthonous Hierodula tenuidentata Saussure, 1869 (Mantodea: Mantidae) from Southeastern Europe, with evidence of its spread across the Pannonian Plain

Natura croatica, 2023-03, Vol.32 (1), p.69-79

2023

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Functional analysis of the novel TBX5c.1333delC mutation resulting in an extended TBX5 protein

BMC medical genetics, 2008-10, Vol.9 (1), Article 88

2008

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Hereditary multiple and isolated sporadic exostoses in the same kindred: identification of the causative gene (EXT2) and detection of a new mutation, nt112delAT, that distinguishes the two phenotypes

International journal of molecular medicine, 2004-01, Vol.13 (1), p.47

2004

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Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescence in situ hybridization

Prenatal diagnosis, 1994-11, Vol.14 (11), p.1019-1028

1994

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Antenatal diagnosis of hereditary fetal growth retardation with aminoaciduria, cholestasis, iron overload, and lactic acidosis in the newborn infant

Acta obstetricia et gynecologica Scandinavica, 2002-05, Vol.81 (5), p.398-402

2002

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Localization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locus

American journal of human genetics, 1995-11, Vol.57 (5), p.1104-1113

1995

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Congenital variant Rett syndrome in a girl with terminal deletion of chromosome 3p

Journal of medical genetics, 1999-04, Vol.36 (4), p.343-345

1999

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Localization of the Human Tripeptidyl Peptidase II Gene (TPP2) to 13q32-q33 by Nonradioactive in Situ Hybridization and Somatic Cell Hybrids

Genomics (San Diego, Calif.), 1993-08, Vol.17 (2), p.493-495

1993

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Subtelomeric rearrangements detected in patients with idiopathic mental retardation

American journal of medical genetics, 2002-02, Vol.107 (4), p.275-284

2002

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Novi podaci za faunu muha pršilica (Diptera: Syrphidae) Bosne i Hercegovine

Entomologia Croatica, 2021-12, Vol.20 (1), p.31

2021

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Incompletely Penetrant PKD1 Alleles Mimic the Renal Manifestations of ARPKD

Novel missense mutations in the glycine receptor β subunit gene ( GLRB ) in startle disease

Mutations in SPINT2 Cause a Syndromic Form of Congenital Sodium Diarrhea

Identification of the gene responsible for Best macular dystrophy

The first arrival of the Chinese sand roach Polyphaga cf. plancyi (Blattodea: Corydiidae) in Europe

The first confirmed record of Mediterranean mantis, Iris oratoria (Mantodea: Eremiaphilidae) in Montenegro

Functional analysis of the novel TBX5 c.1333delC mutation resulting in an extended TBX5 protein

Distribution of genus Libelloides Schaeffer, 1766 (Neuroptera: Ascalaphidae) in Serbia with the help of citizen science

A new greenhouse invader: the first report of the alien ring-legged earwig, Euborellia annulipes (Dermaptera, Anisolabididae) in Serbia, with the first checklist of earwigs of the country

Six new hoverfly species (Diptera: Syrphidae) in the fauna of Serbia

New records and distribution of species from genus Arctophila schiner, 1860 (Diptera: Syrphidae: Eristalinae) in Serbia

The first record of the wharf borer Nacerdes melanura (Linnaeus, 1758) (Coleoptera: Oedemeridae) in Serbia

A case report of two male siblings with autism and duplication of Xq13–q21, a region including three genes predisposing for autism

Functional analysis of the novel TBX5 c. 1333delC mutation resulting in an extended TBX5 protein

First record of the genus Xeropicta Monterosato, 1892 (Gastropoda: Eupulmonata: Geomitridae) in Serbia

New records of allochthonous Hierodula tenuidentata Saussure, 1869 (Mantodea: Mantidae) from Southeastern Europe, with evidence of its spread across the Pannonian Plain

Functional analysis of the novel TBX5c.1333delC mutation resulting in an extended TBX5 protein

Hereditary multiple and isolated sporadic exostoses in the same kindred: identification of the causative gene (EXT2) and detection of a new mutation, nt112delAT, that distinguishes the two phenotypes

Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescence in situ hybridization

Antenatal diagnosis of hereditary fetal growth retardation with aminoaciduria, cholestasis, iron overload, and lactic acidosis in the newborn infant

Localization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locus

Congenital variant Rett syndrome in a girl with terminal deletion of chromosome 3p

Localization of the Human Tripeptidyl Peptidase II Gene (TPP2) to 13q32-q33 by Nonradioactive in Situ Hybridization and Somatic Cell Hybrids

Subtelomeric rearrangements detected in patients with idiopathic mental retardation

Novi podaci za faunu muha pršilica (Diptera: Syrphidae) Bosne i Hercegovine

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