Ten years of experience in molecular prenatal diagnosis and carrier testing for spinal muscular atrophy among families from Serbia

Abstract Objective To describe 10 years of experience of prenatal analysis of spinal muscular atrophy (SMA). Methods Data were retrospectively evaluated from prenatal analysis and carrier screening among parents and close relatives between January 2003 and December 2012. Screening was done before th...

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Veröffentlicht in:	International journal of gynecology and obstetrics 2014-01, Vol.124 (1), p.55-58
Hauptverfasser:	Miskovic, Marijana, Lalic, Tanja, Radivojevic, Danijela, Cirkovic, Sanja, Ostojic, Slavica, Guc-Scekic, Marija
Format:	Artikel
Sprache:	eng
Schlagworte:	Carrier testing Female Genetic Carrier Screening Homozygous deletions Humans Male Molecular Diagnostic Techniques Obstetrics and Gynecology Pregnancy Prenatal Diagnosis Retrospective Studies Serbia - epidemiology SMN1 Spinal Muscular Atrophies of Childhood - diagnosis Spinal Muscular Atrophies of Childhood - epidemiology Spinal Muscular Atrophies of Childhood - genetics spinal muscular atrophy Survival of Motor Neuron 1 Protein - genetics
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