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Publications by Gordana Sosic

The Monosomy 18p Detected by the Amniocentesis: De Grouchy Syndrome 1

Medicinski Casopis

English

Related publications

Monosomy 18p

Orphanet Journal of Rare Diseases

English

Partial Monosomy 13q and Partial Trisomy 18p: Case Report With Necropsy Findings.

Journal of Medical Genetics

English

An Adult Patient With Monosomy 18p, Growth Hormone Deficiency and Selective IgA Deficiency

Journal of Genetic Syndromes & Gene Therapy

English

Spectrum of Movement Disorders in 18p Deletion Syndrome

Movement Disorders Clinical Practice

English

12. Chromosomal Abnormalities Detected by Prenatal Diagnosis by Chorionic Villus Sampling and Amniocentesis, NSW 1998-2000

New South Wales Public Health Bulletin

English

ATR-16 Syndrome: Mechanisms Linking Monosomy to Phenotype

Journal of Medical Genetics

English

Supplemental Information 1: CRISPR Arrays in the Genomes Detected Uniquely by CRT

English

18p--Syndrome Resulting From Translocation (13a;18q) in a Mildly Affected Adult Male.

Journal of Medical Genetics

English

Towards Mapping Phenotypical Traits in 18p− Syndrome by Array-Based Comparative Genomic Hybridisation and Fluorescent in Situ Hybridisation

European Journal of Human Genetics

English