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Bird TD | 25/04/2024Initial Posting: September 28, 1998; Last Revision: April 25, 2024. 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 followi[...]Article
Bird TD | 21/03/2024Initial Posting: September 17, 1999; Last Revision: March 21, 2024. Clinical characteristics. Myotonic dystrophy type 1 (DM1) is a multisystem disorder that affects skeletal and smooth muscle as well as the eye, heart, endocrine system, an[...]Article
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Moller B ; Coppolla A ; Jungbluth H ; Dafsari HS | Seattle (WA) : University of Washington, Seattle | 14/03/2024CLINICAL CHARACTERISTICS: DYNC1H1-related disorders are primarily characterized by an axonal neuropathy with a wide phenotypic spectrum ranging from a neuromuscular-only phenotype (DYNC1H1-related neuromuscular disorder, or DYNC1H1-NMD) to pheno[...]Article
Beijer D ; Marte S ; Li JC ; De Ridder W ; Chen JZ ; Tadenev ALD ; Miers KE ; Deconinck T ; Macdonell R ; Marques W ; De Jonghe P ; Pratt SL ; Meyer-Schuman R ; Zuchner S ; Antonellis A ; Burgess RW ; Baets J | 08/03/2024Article
Favier M ; Delanne J ; Gorincour G ; Faivre L ; Racine C ; Philippe C ; Duffourd Y ; Vitobello A ; Rousseau T ; Martz O ; Tarris G ; Oualiken C ; Thauvin-Robinet C ; Mau-Them FT | 11/02/2024Article
Zanoteli E ; Araujo APQC ; Becker MM ; Fortes CPDD ; França MC ; Machado-Costa MC ; Marques W ; Matsui C ; Mendonça RH ; Nardes F ; Oliveira ASB ; Pessoa ALS ; Saute JAM ; Sgobbi P ; Van der Linden H ; Gurgel-Giannetti J | 01/2024Article
Altassan R ; AlQudairy H ; AlJebreen S ; AlMuhaizea M ; Al-Hindi H ; Pena-Guerra KA ; Ghebeh H ; Almzroua A ; Albakheet A ; AlDosary M ; Colak D ; Arold ST ; Kaya N | 21/12/2023Article
Initial Posting: August 31, 2007; Last Revision: November 2, 2023. Clinical characteristics. Pompe disease is classified by age of onset, organ involvement, severity, and rate of progression. Infantile-onset Pompe disease (IOPD; indiv[...]Article
Wallace SE ; Gillentine MA | 19/10/2023Initial Posting: December 8, 2022; Last Revision: October 19, 2023. A founder variant is a pathogenic variant observed at high frequency in a specific population due to the presence of the variant in a single ancestor or small number of ances[...]Article
Last Update: August 22, 2023. [Previous version: 2020]Article
Leslie ND ; Saenz-Ayala S | 13/07/2023In: Adam MP, Mirzaa GM, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993 Initial Posting: May 28, 2009; Last Revision: July 13, 2023 (Previous Update: June 16, 2022) CLINICAL CHARACT[...]Article
Sangadala S ; Shore EM ; Xu M ; Bergwitz C ; Lozano-Calderon SA ; Lin AE ; Boden SD ; Kaplan FS | 23/05/2023Article
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De Ridder W ; de Vries G ; Van Schil K ; Deconinck T ; Mouly V ; Straub V ; Baets J | England | 07/04/2023Article
Ghaoui R ; Ha TT ; Kerkhof J ; McConkey H ; Gao S ; Babic M ; King R ; Ravenscroft G ; Koszyca B ; Otto S ; Laing NG ; Scott H ; Sadikovic B ; Kassahn KS | 04/04/2023Article
In: Adam MP, Mirzaa GM, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2023. Initial Posting: March 30, 2023. CLINICAL CHARACTERISTICS: CHKB-related muscular dystrophy (CHKB-MD), r[...]Article
Abaji M ; Mignon-Ravix C ; Gorokhova S ; Cacciagli P ; Mortreux J ; Molinari F ; Chabrol B ; Sigaudy S ; Villard L ; Riccardi F | England | 27/03/2023Article
Folland C ; Ganesh V ; Weisburd B ; McLean C ; Kornberg AJ ; O'Donnell-Luria A ; Rehm HL ; Stevanovski I ; Chintalaphani SR ; Kennedy P ; Deveson IW ; Ravenscroft G | United States | 14/03/2023Article
Kramer JJ ; Boon HTM ; Leijten QH ; Ter Laak H ; Eshuis L ; Kusters B ; van Doorn JLM ; Kamsteeg EJ ; Eymard B ; Doorduin J ; Voermans NC | 29/12/2022Article
La Spada A | 15/12/2022Initial Posting: February 26, 1999; Last Update: December 15, 2022. Clinical characteristics. Spinal and bulbar muscular atrophy (SBMA) is a gradually progressive neuromuscular disorder in which degeneration of lower motor neurons results in[...]