Browsing Rektörlüğe Bağlı Bölümler by Subject "Whole genome linkage analysis"
Now showing items 1-3 of 3
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Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype
(BIOMED CENTRAL LTD, 2013)Background: Klippel-Feil syndrome (KFS) is characterized by the developmental failure of the cervical spine and has two dominantly inherited subtypes. Affected individuals who are the children of a consanguineous marriage ... -
Neural tube defect family with recessive trait linked to chromosome 9q21.12-21.31
(SPRINGER, 2015)Meningomyelocele is one of the most common and socioeconomically, psychologically, and physically debilitating neurodevelopmental diseases. A few chromosomal locus and genes have been identified as responsible for the ... -
A Novel Locus for Restless Legs Syndrome on Chromosome 13q
(KARGER, 2012)Background: Restless legs syndrome (RLS) is a sensorimotor disorder in which affected individuals suffer from uncomfortable sensations and an urge to move their lower limbs; it occurs mainly in resting situations during ...