Results 111 to 120 of about 6,833 (235)

Novel familial <i>KDF1</i> mutation detected in members of a three-generation family with clinical manifestations of ectodermal dysplasia: A report of four cases. [PDF]

open access: yesBiomed Rep
Keramida C   +11 more
europepmc   +1 more source

Makarios/Symeon in östlicher Überlieferung

open access: yes, 2019
Seit Jahrzehnten treffen sich vorrangig deutsche und finnische Forscher zu einem Symposium, bei dem die neuesten Forschungsergebnisse und Hypothesen zu Makarios diskutiert werden. Jedes Symposium setzt dabei einen thematischen Schwerpunkt. Abwechselnd wird in Finnland oder in Deutschland getagt.
openaire   +1 more source

Severe Hereditary Hypofibrinogenemia in Pregnancy: A Case Report of a Novel Obstetrical Management with Thromboelastometry Guided Fibrinogen Supplementation. [PDF]

open access: yesDiagnostics (Basel)
Karampas G   +13 more
europepmc   +1 more source

Breaking Bad News During Prenatal Screening: The Role of Professional Obstetricians and Midwives in Greece. [PDF]

open access: yesCureus
Glynou A   +9 more
europepmc   +1 more source

Prenatal Ultrasound Screening and Women's Expectations: an Original Study. [PDF]

open access: yesMater Sociomed, 2022
Glynou A   +10 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy