The role of A2ML1 variants in Noonan syndrome remains unverified

J. Brinkmann; C. Lissewski; V. Pinna; Y. Vial; F. Pantaleoni; F. Lepri; P. Daniele; B. Burnyte; G. Cuturilo; C. Fauth; D. Kotzot; E. Y. Gulec; V. Iotova; G. Forzano; D. Schanze; F. Ramond; M. Havlovicova; G. E. Utine; P. O. Simsek-Kiper; A. Verloes; A. De Luca; M. Tartaglia; H. Cave; M. Zenker

The role of A2ML1 variants in Noonan syndrome remains unverified

J. Brinkmann
, C. Lissewski
, V. Pinna
, Y. Vial
, F. Pantaleoni
, F. Lepri
, P. Daniele
, B. Burnyte
, G. Cuturilo
, C. Fauth
, D. Kotzot
, E. Y. Gulec
, V. Iotova
, G. Forzano
, D. Schanze
, F. Ramond
, M. Havlovicova
, G. E. Utine
, P. O. Simsek-Kiper
, A. Verloes

A. De Luca, M. Tartaglia, H. Cave, M. Zenker

University Hospital Magdeburg
IRCCS Ospedale Casa Sollievo della Sofferenza - San Giovanni Rotondo (FG)
Assistance Publique Hopitaux Paris (APHP)
Institut National de la Sante et de la Recherche Medicale (Inserm)
IRCCS Bambino Gesu
Vilnius University
University of Belgrade
Innsbruck Medical University
Istanbul Kanuni Sultan Suleyman Training and Research Hospital
Medical University of Varna
University of Florence
CHU de St Etienne
Charles University Prague
Motol University Hospital
Hacettepe University

Araştırma sonucu: Dergiye katkı › Toplantı Özeti › bilirkişi

Orijinal dil	İngilizce
Sayfa (başlangıç-bitiş)	479-479
Sayfa sayısı	1
Dergi	European Journal of Human Genetics
Hacim	28
Basın numarası	SUPPL 1
Yayın durumu	Yayınlandı - Ara 2020

Diger dosyalar ve linkler

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Bundan alıntı yap

Brinkmann, J., Lissewski, C., Pinna, V., Vial, Y., Pantaleoni, F., Lepri, F., Daniele, P., Burnyte, B., Cuturilo, G., Fauth, C., Kotzot, D., Gulec, E. Y., Iotova, V., Forzano, G., Schanze, D., Ramond, F., Havlovicova, M., Utine, G. E., Simsek-Kiper, P. O., ... Zenker, M. (2020). The role of A2ML1 variants in Noonan syndrome remains unverified. European Journal of Human Genetics, 28(SUPPL 1), 479-479.

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title = "The role of A2ML1 variants in Noonan syndrome remains unverified",

author = "J. Brinkmann and C. Lissewski and V. Pinna and Y. Vial and F. Pantaleoni and F. Lepri and P. Daniele and B. Burnyte and G. Cuturilo and C. Fauth and D. Kotzot and Gulec, \{E. Y.\} and V. Iotova and G. Forzano and D. Schanze and F. Ramond and M. Havlovicova and Utine, \{G. E.\} and Simsek-Kiper, \{P. O.\} and A. Verloes and \{De Luca\}, A. and M. Tartaglia and H. Cave and M. Zenker",

year = "2020",

month = dec,

language = "English",

volume = "28",

pages = "479--479",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

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Brinkmann, J, Lissewski, C, Pinna, V, Vial, Y, Pantaleoni, F, Lepri, F, Daniele, P, Burnyte, B, Cuturilo, G, Fauth, C, Kotzot, D, Gulec, EY, Iotova, V, Forzano, G, Schanze, D, Ramond, F, Havlovicova, M, Utine, GE, Simsek-Kiper, PO, Verloes, A, De Luca, A, Tartaglia, M, Cave, H & Zenker, M 2020, 'The role of A2ML1 variants in Noonan syndrome remains unverified', European Journal of Human Genetics, hac. 28, no. SUPPL 1, pp. 479-479.

TY - JOUR

T1 - The role of A2ML1 variants in Noonan syndrome remains unverified

AU - Brinkmann, J.

AU - Lissewski, C.

AU - Pinna, V.

AU - Vial, Y.

AU - Pantaleoni, F.

AU - Lepri, F.

AU - Daniele, P.

AU - Burnyte, B.

AU - Cuturilo, G.

AU - Fauth, C.

AU - Kotzot, D.

AU - Gulec, E. Y.

AU - Iotova, V.

AU - Forzano, G.

AU - Schanze, D.

AU - Ramond, F.

AU - Havlovicova, M.

AU - Utine, G. E.

AU - Simsek-Kiper, P. O.

AU - Verloes, A.

AU - De Luca, A.

AU - Tartaglia, M.

AU - Cave, H.

AU - Zenker, M.

PY - 2020/12

Y1 - 2020/12

UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=performanshacettepe&SrcAuth=WosAPI&KeyUT=WOS:000598482601443&DestLinkType=FullRecord&DestApp=WOS_CPL

M3 - Meeting Abstract

SN - 1018-4813

VL - 28

SP - 479

EP - 479

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - SUPPL 1

ER -