5 Einträge gefunden

1. Biallelic PAN2 variants in individuals with a syndromic neurodevelopmental disorder and multiple congenital anomalies

   1. Reuter, Miriam S
   2. Zech, Michael
   3. Hempel, Maja
   4. Altmüller, Janine
   5. Heung, Tracy
   6. Pölsler, Laura
   7. Santer, René

   2022 - Forschungsinformationssystem des UKE
2. A novel homozygous synonymous variant further expands the phenotypic spectrum of POLR3A-related pathologies

   1. Lessel, Davor
   2. Rading, Katrin
   3. Campbell, Susan E
   4. Thiele, Holger
   5. Altmüller, Janine
   6. Gordon, Leslie B
   7. Kubisch, Christian

   2022 - Forschungsinformationssystem des UKE - frei zugänglich
3. ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of-function variants

   1. Kloth, Katja
   2. Lozic, Bernarda
   3. Tagoe, Julia
   4. Hoffer, Mariëtte J V
   5. Van der Ven, Amelie
   6. Thiele, Holger
   7. Altmüller, Janine

   2021 - Forschungsinformationssystem des UKE - frei zugänglich
4. Exome sequencing identifies a novel heterozygous TGFB3 mutation in a disorder overlapping with Marfan and Loeys-Dietz syndrome

   1. Kuechler, Alma
   2. Altmüller, Janine
   3. Nürnberg, Peter
   4. Kotthoff, Stefan
   5. Kubisch, Christian
   6. Borck, Guntram

   2015 - Forschungsinformationssystem des UKE
5. STIL mutation causes autosomal recessive microcephalic lobar holoprosencephaly

   1. Kakar, Naseebullah
   2. Ahmad, Jamil
   3. Morris-Rosendahl, Deborah J
   4. Altmüller, Janine
   5. Friedrich, Katrin
   6. Barbi, Gotthold
   7. Nürnberg, Peter

   2015 - Forschungsinformationssystem des UKE