-
First being described and
identified in 1985,
Wieacker-Wolff
syndrome is a rare,
slowly progressive,
genetic disorder present at
birth and characterized...
- doi:10.1186/s13023-020-01491-9. PMC 7439721. PMID 32819397.
Ledig S,
Wieacker P (2018). "Clinical and
genetic aspects of Mayer–Rokitansky–Küster–Hauser...
- ****ation
White sponge nevus Whooping cough (Pertussis) Whyte–Murphy
syndrome Wieacker syndrome Wiedemann–Grosse–Dibbern
syndrome Wiedemann–Oldigs–Oppermann syndrome...
- 4075–4076. doi:10.1002/ajmg.1320400114. PMID 1909490.
Nieschlag E,
Behre H,
Wieacker P,
Meschede D,
Kamischke A,
Kliesch S (2010). "Disorders at the Testicular...
- PMID 20138711. Wieland, I.; Muschke, P; Jakubiczka, S; Volleth, M; Freigang, B;
Wieacker, PF; et al. (2004). "Refinement of the
deletion in 7q21.3 ****ociated with...
- malformations. The
expression of the ZC4H2
mutation is
referred by some as "
Wieacker-Wolff Syndrome" in
other publications appearing as "Miles-Carpenter Syndrome"...
- PMID 9046242. S2CID 44679684.
Ledig S,
Brucker S,
Barresi G,
Schomburg J, Rall K,
Wieacker P (Sep 2012). "Frame
shift mutation of LHX1 is ****ociated with...
- Röpke, Albrecht; Tewes, Ann-Christin; Gromoll, Jörg; Kliesch, Sabine;
Wieacker, Peter; Tüttelmann,
Frank (9
January 2013). "Comprehensive
sequence analysis...
- Petra; Cohen, Monika; Thiele, Hannelore; Gerlach,
Klaus L.; Adams, Ralf H.;
Wieacker,
Peter (2024-03-14). "Mutations of the Ephrin-B1 Gene
Cause Craniofrontonasal...
-
Stamm T,
Spaich C,
Haase C,
Spree K, Hehr U,
Hoffmann M,
Ledig S, Sel S,
Wieacker P, Röpke A (July 2009). "WNT10A
mutations are a
frequent cause of a broad...
