Mutations in TGDS associated with additional malformations of the middle fingers and halluces: Atypical Catel-Manzke syndrome in a fetus-Reference-Cited by-同舟云学术

Mutations in TGDS associated with additional malformations of the middle fingers and halluces: Atypical Catel-Manzke syndrome in a fetus

Author:

Schoner Katharina¹,Bald Rainer²,Horn Denise³,Rehder Helga¹⁴,Kornak Uwe³⁵⁶,Ehmke Nadja³⁷^ORCID

Affiliation:

1. Institute of Pathology; Fetal pathology; Philipp University of Marburg; Universitätsklinikum Gießen und Marburg; Standort Marburg Marburg Germany

2. Clinic of Gynecology and Prenatal Medicine; Klinikum Leverkusen; Leverkusen Germany

3. Institute of Medical and Human Genetics; Charité-Universitätsmedizin Berlin; Berlin Germany

4. Institute of Medical Genetics; Medical University of Vienna; Vienna Austria

5. Berlin-Brandenburg Center for Regenerative Therapies − BCRT; Charité-Universitätsmedizin Berlin; Berlin Germany

6. Max Planck Institute for Molecular Genetics; Berlin Germany

7. Berlin Institute of Health (BIH); Berlin Germany

Funder

Charité Universitätsmedizin Berlin

Berlin Institute of Health

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference24 articles.

4. Catel W. 1961 Stuttgart G. Thieme

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