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Showing 1 to 5 of 5 for “"Silver-Russell syndrome"”.

  1. Untersuchungen zur Rolle genetischer Veränderungen in der chromosomalen Region 11p15 bei der Entstehung des Silver-Russell-Syndroms

    Silver-Russell-Syndrome (SRS) is a clinically heterogeneous syndrome, associated with pre- and postnatal growth retardation, cranial dysmorphisms, clinodactyly of the fifth finger, skeletal asymmetry and relative macrocephaly. The syndrome usually occurs sporadically, but in some cases a familial …

    aachen Repository record for Untersuchungen zur Rolle genetischer Veränderungen in der chromosomalen Region 11p15 bei der Entstehung des Silver-Russell-Syndroms (opens in a new tab)

  2. Beitrag genetischer Varianten in den Genen LOT1(ZAC1/PLAGL1) und KCNQ1 zur Ätiologie des Silver-Russell-Syndroms

    … which may play a role in the etiology of the Silver-Russell syndrome (SRS). For this reason, both genes were tested for genomic variations. Furthermore, a quantitative gene-copy analysis for LOT1(ZAC1/PLAGL1) was introduced to identify genomic imbalances. In addition, to characterize the …

    aachen Repository record for Beitrag genetischer Varianten in den Genen LOT1(ZAC1/PLAGL1) und KCNQ1 zur Ätiologie des Silver-Russell-Syndroms (opens in a new tab)

  3. Sex steroid secretion during childhood in males - with focus on prematurity, birth size, and growth patterns

    … In paper I, 11 growth hormone-treated boys with SilverRussell syndrome (SRS) who had reached adult height were included. In paper II, two further patients were added. Data on birth characteristics and growth at 6, 8, 10, 12, 14, and 16 years of age were collected retrospectively. Blood samples …

    goteborg Repository record for Sex steroid secretion during childhood in males - with focus on prematurity, birth size, and growth patterns (opens in a new tab)

  4. Implementierung hochauflösender molekulargenetischer Methoden zur Klärung der Pathophysiologie des Silver-Russell-Syndroms

    Silver Russell syndrome (SRS; OMIM #180860) is a clinically and genetically heterogeneous imprinting disorder characterized by severe pre- and postnatal growth retardation, a relative macrocephaly, a triangular face, asymmetry of the body and/or the limbs, and a clinodactyly of the fifth digits. A …

    aachen Repository record for Implementierung hochauflösender molekulargenetischer Methoden zur Klärung der Pathophysiologie des Silver-Russell-Syndroms (opens in a new tab)

  5. Untersuchung zu (epi)genetischen Veränderungen auf Chromosom 11p15 und ihre funktionelle Relevanz bei Patienten mit Silver-Russell-Syndrom

    Silver-Russell syndrome (SRS) is a heterogenous syndrome which is mainly associated with severe intrauterine and postnatal growth retardation. Typical facial dysmorphisms and further characteristic symptoms can additionally be observed. So far the clinical diagnosis can not be confirmed in all …

    aachen Repository record for Untersuchung zu (epi)genetischen Veränderungen auf Chromosom 11p15 und ihre funktionelle Relevanz bei Patienten mit Silver-Russell-Syndrom (opens in a new tab)