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conseil génétiqueSynonyme(s)genetic counselling ;génétique conseil ;consultation génétique genetic counseling |
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Marion S, Auteur | 04/08/2021Article
Article
Initial Posting: June 8, 2000; Last Update: July 29, 2021.Article
Baumbach-Reardon L ; Hunter JM ; Ahearn ME ; Pfautsch M | 29/07/2021Initial Posting: October 30, 2008; Last Update: July 29, 2021.Article
Brève
Marion S, Auteur | 20/07/2021Article
Weber F | 01/07/2021Initial Posting: July 18, 2003; Last Update: July 1, 2021. Clinical characteristics. Hyperkalemic periodic paralysis (hyperPP) is characterized by attacks of flaccid limb weakness (which may also include weakness of the muscles of the eyes[...]Article
Butterfield RJ | 07/2021Article
Uchôa Cavalcanti EB ; Santos SCL ; Martins CES ; de Carvalho DR ; Rizzo IMPO ; Freitas MCDNB ; da Silva Freitas D ; de Souza FS ; Junior AM ; do Nascimento OJM | United States | 30/06/2021Article
Malfatti E ; Catchpool T ; Nouioua S ; Sihem H ; Fournier E ; Carlier RY ; Cardone N ; Davis MR ; Laing NG ; Sternberg D ; Ravenscroft G | England | 23/06/2021Article
Bos JW ; Groen EJN ; Wadman RI ; Curial CAD ; Molleman NN ; Zegers M ; van Vught PWJ ; Snetselaar R ; Vijzelaar R ; van der Pol WL ; van den Berg LH | 22/06/2021Article
Article
Che WI ; Westerlind H ; Lundberg IE ; Hellgren K ; Kuja-Halkola R ; Holmqvist M | England | 15/06/2021Article
Creary LE ; Gangavarapu S ; Caillier SJ ; Cavalcante P ; Frangiamore R ; Lie BA ; Bengtsson M ; Harbo HF ; Brauner S ; Hollenbach JA ; Oksenberg JR ; Bernasconi P ; Maniaol AH ; Hammarström L ; Mantegazza R ; Fernández-Viña MA | 07/06/2021Article
Töpf A ; Pyle A ; Griffin H ; Matalonga L ; Schon K ; Sickmann A ; Schara-Schmidt U ; Hentschel A ; Chinnery PF ; Kolbel H ; Roos A ; Horvath R | England | 01/06/2021Article
Matalonga L ; Hernandez-Ferrer C ; Piscia D ; Schule R ; Synofzik M ; Töpf A ; Vissers LELM ; de Voer R ; Tonda R ; Laurie S ; Fernandez-Callejo M ; Picó D ; Garcia-Linares C ; Papakonstantinou A ; Corvo A ; Joshi R ; Diez H ; Gut I ; Hoischen A ; Graessner H ; Beltran S | England | 01/06/2021Article
Aoki M ; Takahashi T | 27/05/2021Initial Posting: February 5, 2004; Last Update: May 27, 2021. Clinical characteristics. Dysferlinopathy includes a spectrum of muscle disease characterized by two major phenotypes: Miyoshi muscular dystrophy (MMD) and limb-girdle muscular [...]Article
Bird TD | 20/05/2021Initial Posting: September 28, 1998; Last Revision: September 9, 2021. The purpose of this overview is to increase the awareness of clinicians regarding Charcot-Marie-Tooth (CMT) hereditary neuropathy, its causes, and its management. The f[...]Article
Leslie ND ; Valencia CA ; Strauss AW ; Zhang K | 13/05/2021Initial Posting: May 28, 2009; Last Revision: May 13, 2021. Clinical characteristics. Deficiency of very long-chain acyl-CoA dehydrogenase (VLCAD), which catalyzes the initial step of mitochondrial β-oxidation of long-chain fatty acids wit[...]Article
Article
Over L ; Brüggemann N ; Lohmann K | 13/05/2021Article
[Republished online : 2021 May 13];[Published online : 2020 Dec 7] »Article
Takizawa H ; Mori-Yoshimura M ; Minami N ; Murakami N ; Yatabe K ; Taira K ; Hashimoto Y ; Aoki Y ; Nishino I ; Takahashi Y | England | 27/04/2021Article
Initial Posting: June 11, 2015; Last Update: April 8, 2021 Clinical description. Riboflavin transporter deficiency (RTD), comprising RTD2 and RTD3 (caused by biallelic pathogenic variants in SLC52A2 and SLC52A3, respectively) is a rare neu[...]Article
Kutluk MG ; Kadem N ; Bektas O ; Randa NC ; Tuncer GO ; Albayrak P ; Eminoglu T ; Teber ST | 04/2021
