Miller–Dieker syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Miller–Dieker syndrome" in English language version.

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8nih.gov

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5doi.org

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2semanticscholar.org

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1clevelandclinic.org

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clevelandclinic.org

my.clevelandclinic.org

"Miller-Dieker Syndrome". Cleveland Clinic. Retrieved 14 February 2023.

doi.org

Herman, T E; Siegel, M J (April 2008). "Miller–Dieker syndrome, type 1 lissencephaly". Journal of Perinatology. 28 (4): 313–315. doi:10.1038/sj.jp.7211920. PMID 18379572. S2CID 35782905.
Pollin, TI; Dobyns, WB; Crowe, CA; Ledbetter, DH; Bailey-Wilson, JE; Smith, AC (6 August 1999). "Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3". American Journal of Medical Genetics. 85 (4): 369–75. doi:10.1002/(sici)1096-8628(19990806)85:4<369::aid-ajmg13>3.0.co;2-l. PMID 10398263.
Izumi K, Kuratsuji G, Ikeda K, Takahashi T, Kosaki K (2007). "Partial deletion of LIS1: a pitfall in molecular diagnosis of Miller-Dieker syndrome". Pediatr. Neurol. 36 (4): 258–60. doi:10.1016/j.pediatrneurol.2006.11.015. PMID 17437911.
Chong, SS; Pack, SD; Roschke, AV; Tanigami, A; Carrozzo, R; Smith, AC; Dobyns, WB; Ledbetter, DH (February 1997). "A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3". Human Molecular Genetics. 6 (2): 147–55. doi:10.1093/hmg/6.2.147. PMID 9063734.
Miller JQ (1963). "Lissencephaly in 2 siblings". Neurology. 13 (10): 841–50. doi:10.1212/wnl.13.10.841. PMID 14066999. S2CID 42698337.

nih.gov

pubmed.ncbi.nlm.nih.gov

Huang, HC; Bautista, SL; Chen, BS; Chang, KP; Chen, YJ; Wuu, SW (1996). "Miller-Dieker syndrome with microdeletion of chromosome 17p13.3: report of one case". Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui. 38 (6): 472–6. PMID 9473821.
Herman, T E; Siegel, M J (April 2008). "Miller–Dieker syndrome, type 1 lissencephaly". Journal of Perinatology. 28 (4): 313–315. doi:10.1038/sj.jp.7211920. PMID 18379572. S2CID 35782905.
Dobyns, WB; Das, S; Pagon, RA; Adam, MP; Ardinger, HH; Wallace, SE; Amemiya, A; Bean, LJH; Bird, TD; Dolan, CR; Fong, CT; Smith, RJH; Stephens, K (1993). "PAFAH1B1-Related Lissencephaly/Subcortical Band Heterotopia". PAFAH1B1-Associated Lissencephaly/Subcortical Band Heterotopia. University of Washington, Seattle. PMID 20301752.
Pollin, TI; Dobyns, WB; Crowe, CA; Ledbetter, DH; Bailey-Wilson, JE; Smith, AC (6 August 1999). "Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3". American Journal of Medical Genetics. 85 (4): 369–75. doi:10.1002/(sici)1096-8628(19990806)85:4<369::aid-ajmg13>3.0.co;2-l. PMID 10398263.
Izumi K, Kuratsuji G, Ikeda K, Takahashi T, Kosaki K (2007). "Partial deletion of LIS1: a pitfall in molecular diagnosis of Miller-Dieker syndrome". Pediatr. Neurol. 36 (4): 258–60. doi:10.1016/j.pediatrneurol.2006.11.015. PMID 17437911.
Chong, SS; Pack, SD; Roschke, AV; Tanigami, A; Carrozzo, R; Smith, AC; Dobyns, WB; Ledbetter, DH (February 1997). "A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3". Human Molecular Genetics. 6 (2): 147–55. doi:10.1093/hmg/6.2.147. PMID 9063734.
Miller JQ (1963). "Lissencephaly in 2 siblings". Neurology. 13 (10): 841–50. doi:10.1212/wnl.13.10.841. PMID 14066999. S2CID 42698337.

ncbi.nlm.nih.gov

Dobyns, WB; Das, S; Pagon, RA; Adam, MP; Ardinger, HH; Wallace, SE; Amemiya, A; Bean, LJH; Bird, TD; Dolan, CR; Fong, CT; Smith, RJH; Stephens, K (1993). "PAFAH1B1-Related Lissencephaly/Subcortical Band Heterotopia". PAFAH1B1-Associated Lissencephaly/Subcortical Band Heterotopia. University of Washington, Seattle. PMID 20301752.

semanticscholar.org

api.semanticscholar.org

Herman, T E; Siegel, M J (April 2008). "Miller–Dieker syndrome, type 1 lissencephaly". Journal of Perinatology. 28 (4): 313–315. doi:10.1038/sj.jp.7211920. PMID 18379572. S2CID 35782905.
Miller JQ (1963). "Lissencephaly in 2 siblings". Neurology. 13 (10): 841–50. doi:10.1212/wnl.13.10.841. PMID 14066999. S2CID 42698337.