• Somatic evolution is the accumulation of mutations and epimutations in somatic cells (the cells of a body, as opposed to germ plasm and stem cells) during...
    87 KB (9,928 words) - 12:18, 13 August 2024
  • Thumbnail for Strawberry roan
    ISBN 978-1-78639-258-9. Marandet, Laure (2018). Les robes des chevaux : Approche génétique et scientifique des robes des chevaux. Cheval pratique (in French). Italy:...
    34 KB (3,708 words) - 22:10, 2 July 2024
  • Thumbnail for XX male syndrome
    positive XX maleness: a case report and review of literature". Annales de Génétique. 46 (1): 11–18. doi:10.1016/S0003-3995(03)00011-X. PMID 12818524. Rajender...
    27 KB (2,977 words) - 23:15, 11 October 2024
  • Thumbnail for Frank–Ter Haar syndrome
    with multiple skeletal anomalies: a new genetic syndrome?". Journal de génétique humaine. 21 (2): 67–72. PMID 4805907. Ter Haar B, Hamel B, Hendriks J...
    5 KB (510 words) - 04:19, 16 May 2022
  • Thumbnail for Mitochondrial DNA
    PMID 23704099. Boursot P, Bonhomme F (1 January 1986). "[Not Available]". Génétique, Sélection, Évolution. 18 (1): 73–98. doi:10.1186/1297-9686-18-1-73. PMC 2713894...
    95 KB (10,005 words) - 15:44, 16 October 2024
  • Thumbnail for Microsatellite instability
    Microsatellite instability (category Mutation)
    instability (MSI) is the condition of genetic hypermutability (predisposition to mutation) that results from impaired DNA mismatch repair (MMR). The presence of...
    25 KB (3,091 words) - 20:05, 22 September 2024
  • Thumbnail for Autism in France
    d'information : Autisme". Inserm. Inserm (2012). "Autisme : des mutations génétiques perturbent la communication entre les neurones". Inserm. Archived...
    187 KB (21,096 words) - 23:52, 29 August 2024
  • Thumbnail for Lujan–Fryns syndrome
    "Chromosome X-linked mental retardation and marfanoid syndrome". Journal de Génétique Humaine. 36 (1–2): 123–128. ISSN 0021-7743. PMID 3379374. Mégarbané A...
    40 KB (4,178 words) - 03:02, 17 September 2024
  • Thumbnail for Jean Rostand
    et génération, 1940 - Science and generation Les idées nouvelles de la génétique, 1941 - New ideas in genetics L’Homme, introduction à l’étude de la biologie...
    14 KB (1,509 words) - 06:07, 12 April 2024
  • Interview de Stasnislas Lyonne. Génétique et embryologie... Imagine. Stanislas Lyonnet, Prix Recherche 2009. Sources "Génétique et embryologie des malformations...
    7 KB (884 words) - 20:06, 27 October 2023
  • Thumbnail for Malagasy peoples
    Researchgate. "Madagascar, illustration inédite de la mondialisation génétique | INEE". inee.cnrs.fr (in French). August 2017. Retrieved 2021-02-25....
    18 KB (1,836 words) - 14:23, 10 October 2024
  • Thumbnail for Epigenetics
    December 2013. Morange M. La tentative de Nikolai Koltzoff (Koltsov) de lier génétique, embryologie et chimie physique, J. Biosciences. 2011. V. 36. P. 211-214...
    161 KB (18,346 words) - 02:11, 20 August 2024
  • Thumbnail for Vitiligo
    Twitter. Prisma MP (11 June 2018). "Michaël Youn : l'étonnante maladie génétique dont il est atteint… au niveau du pénis - Voici". Voici.fr (in French)...
    42 KB (4,420 words) - 06:35, 20 October 2024
  • Thumbnail for Preimplantation genetic diagnosis
    Stephan (2008). "Création et destruction de la diversité génétique dans une population". Génétique statistique. pp. 77–106. doi:10.1007/978-2-287-33911-0_4...
    111 KB (14,613 words) - 17:14, 20 September 2024
  • Thumbnail for Hand clasping
    1080/030144699282967. PMID 9974082. Leguebe 1967 hand clasping: étude anthropologique et génétique. Bull. Soc. Roy. Antrop. Préhist., 78: 81-107. Hadžiselimović, R.; Berberović...
    15 KB (1,584 words) - 21:09, 12 August 2024
  • Thumbnail for Beckwith–Wiedemann syndrome
    with umbilical hernia and macroglossia - a "new syndrome"?". Journal de Génétique Humaine (in French). 13: 223–32. PMID 14231762. "John Bruce Beckwith"...
    31 KB (3,949 words) - 01:58, 3 September 2024
  • supervision of J Robert S Whittle before moving to the Laboratoire de Génétique Moleculaire des Eukaryotes in Strasbourg, France, as a Royal Society European...
    9 KB (974 words) - 08:46, 4 October 2024
  • Thumbnail for Napoleon Oak (Lausanne)
    Emmanuel (12 April 2017). "Le chêne de Napoléon défie les postulats de la génétique". 24Heures (in French). "Le chêne – Napoleome". www.napoleome.ch (in French)...
    4 KB (369 words) - 23:20, 28 April 2024
  • Thumbnail for Limousin cattle
    LA BELLE LIMOUSINE. La vache limousine, un patrimoine historique et génétique. Limoges: Culture et patrimoine en Limousin. ISBN 978-2-911167-39-3. L...
    86 KB (10,454 words) - 18:32, 17 September 2024
  • Thumbnail for Emberger syndrome
    caused by familial or sporadic inactivating mutations in one of the two parental GATA2 genes. The mutation results in a haploinsufficiency (i.e. reduction)...
    22 KB (2,579 words) - 15:05, 25 September 2021
  • autonomic dysfunction. The disorder has been associated with various mutations in the SLC52A2 and SLC52A3 genes. This gene is thought to be involved...
    13 KB (1,465 words) - 14:19, 28 July 2024
  • Thumbnail for Bernard Dujon
    Pasteur, then Professor from 1993 to 2015. He was the head of the Unité de Génétique Moléculaire des Levures from 1989 to his retirement in 2015. Among the...
    33 KB (3,908 words) - 20:38, 18 October 2024
  • Feingold. In 2007, she became director of the Laboratoire de Psychiatrie Génétique, a laboratory renamed "Laboratoire de Neuro-Psychiatrie Translationnelle"...
    38 KB (3,969 words) - 18:13, 30 July 2024
  • Thumbnail for Cheikh Anta Diop
    Dakar: IFAN. Initiations et études Africaines no. 31. (1977) Parenté génétique de l'égyptien pharaonique et des langues négro-africaines: processus de...
    36 KB (4,445 words) - 16:43, 7 October 2024
  • Thumbnail for Factor X
    (August 1995). "Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the...
    27 KB (3,353 words) - 09:39, 12 August 2024
  • sélection de variables en régression en grande dimension: Application en génétique animale (Thesis) (in French). Lille University of Science and Technology...
    58 KB (6,933 words) - 03:15, 11 March 2024
  • Thumbnail for Microlissencephaly
    suggesting an autosomal recessive inheritance. Mutation of RELN gene or CIT could cause MLIS. Human NDE1 mutations and mouse Nde1 loss lead to cortical lamination...
    29 KB (2,704 words) - 14:13, 18 July 2024
  • Thumbnail for Maxime Schwartz
    353-356, 2014 C. Vincent, Mort de François Jacob, pionnier du génie génétique, Le Monde. fr., 21 avril 2013. [archive] "Académie des sciences". Décret...
    13 KB (1,783 words) - 18:28, 27 September 2023
  • Thumbnail for Yunis–Varon syndrome
    recessive manner. Several mutations in the FIG4-encoding gene were found to cause Yunis–Varon syndrome. Some of these mutations result in complete loss...
    28 KB (2,976 words) - 21:47, 26 November 2023
  • Thumbnail for PQBP1
    non-specific X-linked mental retardation (MRX55) is located in Xp11". Annales de Génétique. 41 (1): 11–16. PMID 9599645. Komuro A, Saeki M, Kato S (May 1999). "Npw38...
    28 KB (3,107 words) - 00:17, 13 August 2024