Kleefstra-szindróma (Hungarian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Kleefstra-szindróma" in Hungarian language version.

refsWebsite

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3,537^th place

7,492^nd place

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1,167^th place

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8^th place

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4,380^th place

low place

bmj.com

jmg.bmj.com

Kleefstra, T, W M (2009. szeptember 1.). „Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype” (angol nyelven). Journal of Medical Genetics 46 (9), 598–606. o. DOI:10.1136/jmg.2008.062950. ISSN 0022-2593.

doi.org

dx.doi.org

Kleefstra, T, W M (2009. szeptember 1.). „Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype” (angol nyelven). Journal of Medical Genetics 46 (9), 598–606. o. DOI:10.1136/jmg.2008.062950. ISSN 0022-2593.

omim.org

OMIM Entry - # 610253 - KLEEFSTRA SYNDROME 1; KLEFS1. omim.org. (Hozzáférés: 2020. július 5.)

orpha.net

Orphanet: Search a disease. www.orpha.net. (Hozzáférés: 2020. július 5.)

worldcat.org

Kleefstra, T, W M (2009. szeptember 1.). „Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype” (angol nyelven). Journal of Medical Genetics 46 (9), 598–606. o. DOI:10.1136/jmg.2008.062950. ISSN 0022-2593.