Disomia uniparentale (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Disomia uniparentale" in Italian language version.

refsWebsite

Global rank Italian rank

4^th place

9^th place

2^nd place

7^th place

799^th place

22^nd place

6^th place

8^th place

5^th place

26^th place

4,963^rd place

325^th place

87^th place

low place

1web.archive.org

1^st place

1^st place

4,380^th place

4,368^th place

1diseasesdatabase.com

low place

low place

archive.is

(EN) Arpan Bhatt, Thomas Liehr, Sonal R. Bakshi, Phenotypic spectrum in uniparental disomy: Low incidence or lack of study, in Indian Journal of Human Genetics, vol. 19, n. 3, 2013, pp. 131–134, DOI:10.4103/0971-6866.120819, PMID 24339543 (archiviato dall'url originale il 20 febbraio 2014).

archive.org

(EN) Human Molecular Genetics 3, Garland Science, p. 58, ISBN 0-8153-4183-0.
(EN) J.E. Spence et al., Uniparental disomy as a mechanism for human genetic disease, in American Journal of Human Genetics, vol. 42, n. 2, 1988, pp. 217–226, PMID 2893543.

diseasesdatabase.com

(EN) Malcolm Duncan, Chromosome 14 uniparental disomy syndrome information Diseases Database, su www.diseasesdatabase.com, 1º settembre 2020. URL consultato il 1º settembre 2020.

doi.org

dx.doi.org

(EN) W.P. Robinson, <452::AID-BIES7>3.0.CO;2-K Mechanisms leading to uniparental disomy and their clinical consequences, in BioEssays, vol. 22, n. 5, maggio 2000, pp. 452–459, DOI:10.1002/(SICI)1521-1878(200005)22:5<452::AID-BIES7>3.0.CO;2-K, PMID 10797485.
(EN) D.A. King, A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders, in Genome Research, vol. 24, n. 4, 2013, pp. 673–687, DOI:10.1101/gr.160465.113, PMID 24356988.
(EN) Priyanka Nakka et al., Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population, in American Journal of Human Genetics, vol. 105, n. 5, 7 novembre 2019, pp. 921–932, DOI:10.1016/j.ajhg.2019.09.016, ISSN 0002-9297 (WC · ACNP), PMID 31607426.
(EN) Arpan Bhatt, Thomas Liehr, Sonal R. Bakshi, Phenotypic spectrum in uniparental disomy: Low incidence or lack of study, in Indian Journal of Human Genetics, vol. 19, n. 3, 2013, pp. 131–134, DOI:10.4103/0971-6866.120819, PMID 24339543 (archiviato dall'url originale il 20 febbraio 2014).

nih.gov

ncbi.nlm.nih.gov

(EN) W.P. Robinson, <452::AID-BIES7>3.0.CO;2-K Mechanisms leading to uniparental disomy and their clinical consequences, in BioEssays, vol. 22, n. 5, maggio 2000, pp. 452–459, DOI:10.1002/(SICI)1521-1878(200005)22:5<452::AID-BIES7>3.0.CO;2-K, PMID 10797485.
(EN) D.A. King, A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders, in Genome Research, vol. 24, n. 4, 2013, pp. 673–687, DOI:10.1101/gr.160465.113, PMID 24356988.
(EN) Priyanka Nakka et al., Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population, in American Journal of Human Genetics, vol. 105, n. 5, 7 novembre 2019, pp. 921–932, DOI:10.1016/j.ajhg.2019.09.016, ISSN 0002-9297 (WC · ACNP), PMID 31607426.
(EN) Arpan Bhatt, Thomas Liehr, Sonal R. Bakshi, Phenotypic spectrum in uniparental disomy: Low incidence or lack of study, in Indian Journal of Human Genetics, vol. 19, n. 3, 2013, pp. 131–134, DOI:10.4103/0971-6866.120819, PMID 24339543 (archiviato dall'url originale il 20 febbraio 2014).
(EN) J.E. Spence et al., Uniparental disomy as a mechanism for human genetic disease, in American Journal of Human Genetics, vol. 42, n. 2, 1988, pp. 217–226, PMID 2893543.

oadoi.org

(EN) W.P. Robinson, <452::AID-BIES7>3.0.CO;2-K Mechanisms leading to uniparental disomy and their clinical consequences, in BioEssays, vol. 22, n. 5, maggio 2000, pp. 452–459, DOI:10.1002/(SICI)1521-1878(200005)22:5<452::AID-BIES7>3.0.CO;2-K, PMID 10797485.
(EN) D.A. King, A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders, in Genome Research, vol. 24, n. 4, 2013, pp. 673–687, DOI:10.1101/gr.160465.113, PMID 24356988.
(EN) Priyanka Nakka et al., Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population, in American Journal of Human Genetics, vol. 105, n. 5, 7 novembre 2019, pp. 921–932, DOI:10.1016/j.ajhg.2019.09.016, ISSN 0002-9297 (WC · ACNP), PMID 31607426.

omim.org

OMIM 105830

unibo.it

acnpsearch.unibo.it

(EN) Priyanka Nakka et al., Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population, in American Journal of Human Genetics, vol. 105, n. 5, 7 novembre 2019, pp. 921–932, DOI:10.1016/j.ajhg.2019.09.016, ISSN 0002-9297 (WC · ACNP), PMID 31607426.

web.archive.org

(EN) Meiosis: Uniparental Disomy, su peds.ufl.edu. URL consultato il 29 febbraio 2016 (archiviato dall'url originale il 16 maggio 2021).

worldcat.org

(EN) Priyanka Nakka et al., Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population, in American Journal of Human Genetics, vol. 105, n. 5, 7 novembre 2019, pp. 921–932, DOI:10.1016/j.ajhg.2019.09.016, ISSN 0002-9297 (WC · ACNP), PMID 31607426.