A step towards precision medicine in management of severe transient polyhydramnios: MAGED2 variant

Chloé J. Arthuisa Service de Gynécologie et Obstétrique, CHU Nantes, Nantes Cedex, France;

https://orcid.org/0000-0002-7937-3648

Mathilde Nizonb Service de Génétique Médicale, CHU Nantes, Nantes Cedex, France;

Martin Kömhoffc University Children's Hospital, Philipps University Marburg, Marburg, Germany;

Bodo B. Beckd Institute of Human Genetics, University of Cologne, Cologne, Germany; ;e Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany;

Vera Riehmerd Institute of Human Genetics, University of Cologne, Cologne, Germany;

Tiphaine Bihouéef Service de Pédiatrie, CHU Nantes, Nantes, France;

Alexandra Bruelf Service de Pédiatrie, CHU Nantes, Nantes, France;

Nadir Benbrikg Service de Cardiologie Pédiatrique, CHU Nantes, Nantes, France

Norbert Winera Service de Gynécologie et Obstétrique, CHU Nantes, Nantes Cedex, France;

Bertrand Isidorb Service de Génétique Médicale, CHU Nantes, Nantes Cedex, France; Correspondence[email protected]

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References

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A step towards precision medicine in management of severe transient polyhydramnios: MAGED2 variant

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A step towards precision medicine in management of severe transient polyhydramnios: MAGED2 variant

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