Morten Krogh Herlin

13PUBLICATIONS
55CO-AUTHORS
Gene mappingPsychology of ageingDevelopmental genetics (incl. sex determination)Psychosocial aspects of childbirth and perinatal mental healthPolymerisation mechanisms
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Publications (13)

|Sep 28, 2026
Müllerian Duct Aplasia in a Girl With SMARCB1-Related Coffin-Siris Syndrome: A Rare Co-Occurring Anomaly.

|May 12, 2025
Life Beyond Childhood: Insight Into the Lived Experience of 91 Adults With KBG Syndrome Through an Online Patient/Caregiver-Reported Co-Produced Questionnaire.

Karen J Low, Moira Walker, Georgia Treneman-Evans

|Sep 11, 2024
Phenotypes, Genetics, and Estimated Prevalence of Focal Dermal Hypoplasia (Goltz Syndrome): A Single-Center Report.

Laura Krogh Herlin, Morten Krogh Herlin, Hanne Vinter

|Jul 23, 2024
Experiences of vaginal lengthening treatment and sexual well-being in women with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: An interview study.

Amalie Hahn Jensen, Morten Krogh Herlin, Birgitta Trolle

|Jun 12, 2023
Congenital mirror movements are associated with defective polymerisation of RAD51.

Oriane Trouillard, Pauline Dupaigne, Margaux Dunoyer

|Mar 29, 2023
A life course perspective on Mayer-Rokitansky-Küster-Hauser syndrome: women's experiences and negotiations of living with an underdeveloped uterus and vagina.

Amalie Hahn Jensen, Morten Krogh Herlin, Ida Vogel

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Frequent Collaborators

4 joint publications

Linda Holmfeldt

2 joint publications

Isabelle Dusart

2 joint publications

Svea Stratmann

2 joint publications

Jenny Blechingberg