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Domain-Statistiken für "spatax.wordpress.com"

93
Business Relations
92
Eindeutige Domains
20
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BR-Relations: 93
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/2024/09/page/2/
/crmr-neurogene/
/giovanni-stevanin
/actualites/maladies-motoneurone-18-nouveaux-genes-identifies
/2013/04/11/paraplegies-spastiques-hereditaires-des-mutations-dans-3-nouveaux-genes-impliquent-le-metabolisme-des-lipides-dans-la-degenerescence-des-motoneurones/
/2013/11/04/mutations-link-cerebellar-ataxia-spastic-paraplegia-to-lipid-biology/
/2013/12/31/carte-de-voeux-2014-de-linserm/
/2014/02/02/identification-of-18-new-causative-genes-in-hereditary-spastic-paraplegias/
/2014/03/12/an-on-line-survey-covering-mobility-symptoms-resources-and-mis-diagnoses-for-people-with-hereditary-spastic-paraplegia-by-adam-lawrence/
/2014/03/12/an-on-line-survey-covering-mobility-symptoms-resources-and-mis-diagnoses-for-people-with-hereditary-spastic-paraplegia-by-adam-lawrence/
/2012/10/19/september-the-25th-world-day-for-public-awareness-to-ataxia-2/
/2012/10/19/september-the-25th-world-day-for-public-awareness-to-ataxia-2/
/2013/06/22/mancini-et-al-bmc-medical-genomics-2013/
/2013/09/10/breves-scientifiques-de-linserm-paraplegies-spastiques-hereditaires-implication-du-metabolisme-des-gangliosides/
/2014/11/29/severe-dystonia-cerebellar-atrophy-and-cardiomyopathy-likely-caused-by-a-missense-mutation-in-tor1aip1-orphanet-j-rare-dis-2014/
/2014/12/20/spinocerebellar-ataxia-type-36-exists-in-diverse-populations-and-can-be-caused-by-a-short-hexanucleotide-ggcctg-repeat-expansion-jnnp-2014/
/2013/12/12/kif1c-mutations-in-two-families-with-hereditary-spastic-paraparesis-and-cerebellar-dysfunction/
/2013/04/15/draft-agenda-for-euro-hsp-annual-meeting-and-general-assembly/
/2013/06/20/petition-la-recherche-biomedicale-est-en-danger-soutenons-la-par-deux-mesures-simples/
/2013/05/07/914/