Hereditäre Prosopagnosie in Brasilien

Kotzyba, Ferdinand Sebastian
2010

Genetik der kongenitalen Prosopagnosie

Grüter, Martina
2004

Prosopagnosie (syn. Gesichtsblindheit) – Berichte von Betroffenen

Kennerknecht, Ingo
2022

Hereditary prosopagnosia in self reports

Kennerknecht, Ingo, Trostmann, Ulrike
2022

Klinik des 5p-minus Syndroms (syn. Cri-du-Chat Syndrom)

Daten einer Fragebogenerhebung (2010 – 2019)

Kennerknecht, Ingo, Kröll-Schulte, Agnes, Schulte, Hans Reiner
2021

Acquired and hereditary prosopagnosia in history, fiction literature, biographies, and live celebrities of the present

Kennerknecht, Ingo
2022

Extreme founder effect associated with oculocutaneous albinism type 1 (OCA1) on the island of Nias/Indonesia

How clinical genetics may help population genetics

Kennerknecht, Ingo, Zühlke, Christine, Hämmerle, Johannes M.
2021

An intronic COL1A1 Sp1-Polymorphism but not Vitamin D Receptor Gene Polymorphisms Relates to the Phenotypic Expression of Osteogenesis imperfecta

Trummer, Tatjana, Kennerknecht, Ingo
2022

Prevalence of hereditary prosopagnosia – a worldwide survey

Kennerknecht, Ingo, Edwards, Steve D., Van Belle, Goedele, Wang-Elze, Zhi, Wang, Hui, Hämmerle, Johannes M., Aras, Beyhan Durak, Thomas, Claudia, Thomas, Christian
2021

The Sculpted Word

The Gowe Ni'Oniha of Nias

Battais, Yves, Kennerknecht, Ingo
2023

Evaluation eines Fragebogens zum Populationsscreening auf hereditäre Prosopagnosie

Stiefermann, Melissa

X-linked recessive familial gout on the island of Nias/Indonesia

Preliminary results in the context of population genetics field research

Kennerknecht, Ingo, Hämmerle, Johannes Maria
2024

Hereditäre Prosopagnosie

erste Familienbeschreibungen in Finnland

Wentzek, Sebastian
2016

Prospektive Reevaluation eines Fragebogens zum Screening auf hereditäre Prosopagnosie

Winterberg, Vanessa Maria