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Genetic testing in inherited endocrine disorders: joint pos..:

Eggermann, Thomas ; Elbracht, Miriam ; Kurth, Ingo...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13023-020-01420-w. , 2020

Link: https://hal.science/hal-04026146

RT Journal
T1 <Title>Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftccsdartic:oai:HAL:hal-04026146v1&Exemplar=1&LAN=DE
				
A1 Eggermann, Thomas
A1 Elbracht, Miriam
A1 Kurth, Ingo
A1 Juul, Anders
A1 Johannsen, Trine Holm
A1 Netchine, Irène
A1 Mastorakos, George
A1 Johannsson, Gudmundur
A1 Musholt, Thomas, J
A1 Zenker, Martin
A1 Prawitt, Dirk
A1 Pereira, Alberto, M
A1 Hiort, Olaf
A1 Riedl, Stefan
A1 Rami-Merhar, Birgit
A1 Vila, Greisa
A1 Baumgartner-Parzner, Sabina
A1 Bonfig, Walter
A1 Heinrichs, Claudine
A1 Maiter, Dominique
A1 Gies, Inge
A1 Cools, Martine
A1 Casteels, Kristina
A1 Beckers, Albert
A1 Zacharieva, Sabina
A1 Iotova, Violeta
A1 Jukic, Tomislav
A1 Rahelic, Dario
A1 Neocleous, Vassos
A1 Phylactou, Leonidas
A1 Krsek, Michal
A1 Lebl, Jan
A1 Gravholt, Claus
A1 Tillmann, Vallo
A1 Volke, Vallo
A1 Ebeling, Tapani
A1 Brue, Thierry
A1 Rodien, Patrice
A1 Bertherat, Jérôme
A1 Bernert, Christine Poitou
A1 Touraine, Philippe
A1 Chanson, Philippe
A1 Polak, Michel
A1 Tauber, Maithe
A1 Spranger, Joachim
A1 Fuhrer, Dagmar
A1 Danne, Thomas
A1 Mohnike, Klaus
A1 Luster, Markus
A1 Reisch, Nicole
A1 Reincke, Martin
A1 Rohayem, Julia
A1 Fassnacht, Martin
A1 Tóth, Miklós
A1 Cassio, Alessandra
A1 Toni, Sonia
A1 Krausz, Csilla
A1 Piccini, Barbara
A1 Ferone, Diego
A1 Russo, Gianni
A1 Persani, Luca
A1 Colao, Annamaria
A1 Salerno, Mariacarolina
A1 Boscaro, Marco
A1 Scaroni, Carla
A1 Santini, Ferruccio
A1 Ceccarini, Giovanni
A1 Ghigo, Ezio
A1 Dzivite - Krisane, Iveta
A1 Rovite, Vita
A1 Janozola, Lauma
A1 Verkauskiene, Rasa
A1 Witsch, Michael
A1 Clark, James
A1 Romijn, Johannes
A1 Links, Thera
A1 Biermasz, Nienke
A1 Hannema, Sabine
A1 Havekes, Bas
A1 Der Grinten, Hedi Claahsen-Van
A1 Timmers, Henri
A1 Peeters, Robin
A1 Valk, Gerlof
A1 Stuart, A, a Verrijn
A1 Haak, Harm
A1 Husebye, Eystein
A1 Bollerslev, Jens
A1 Jarzab, Barbara
A1 Raposo, João-Filipe
A1 Craiu, Dana
A1 Piciu, Doina
A1 Kostalova, Ludmila
A1 Vojtková, Jarmila
A1 Battelino, Tadej
A1 Cardona-Hernandez, Roque
A1 Yeste, Diego
A1 Gaztambide, Sonia
A1 Nordenström, Anna
A1 Gittoes, Neil
A1 Cole, Trevor
A1 Crowne, Elizabeth
A1 Ahmed, Faisal
A1 Didi, Mohammed
A1 Korbonits, Marta
A1 Dattani, Mehul
A1 Clayton, Peter
A1 Davies, Justin
PB HAL CCSD; BioMed Central
YR 2020
K1 Rare endocrine conditions Genetic testing Imprinting disorders Short stature -glucose and insulin homeostasis -Hypogonadotropic hypogonadism -differences/disorders of sex development
K1 Rare endocrine conditions
K1 Genetic testing
K1 Imprinting disorders
K1 Short stature -glucose and insulin homeostasis -Hypogonadotropic hypogonadism -differences/disorders of sex development
K1 [SDV]Life Sciences [q-bio]
JF info:eu-repo/semantics/altIdentifier/doi/10.1186/s13023-020-01420-w
LK http://dx.doi.org/https://hal.science/hal-04026146
DO https://hal.science/hal-04026146
SF ELIB - SuUB Bremen

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