PubMed for id: 334629

Year	Number of Results
1981	1
1982	1
1984	1
1985	2
1986	1
1987	1
1989	3
1992	6
1993	1
1994	2
1995	5
1996	3
1997	7
1998	2
1999	5
2000	6
2001	7
2002	4
2003	8
2004	9
2005	12
2006	12
2007	6
2008	18
2009	5
2010	11
2011	11
2012	10
2013	11
2014	15
2015	5
2016	14
2017	6
2018	7
2019	4
2020	8
2021	9
2022	3
2023	2

1

[Prenatal diagnosis of two fetuses with chromosome 1p36 deletion syndrome].

Ji X, Hu H, Wang Y, Liang D, Luo C, Meng L, Zhou J, Cao L, Ma D, Hu P, Xu Z. Ji X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):853-856. doi: 10.3760/cma.j.issn.1003-9406.2017.06.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188615 Chinese.

2

Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.

Chen CP, Chen M, Su YN, Hsu CY, Tsai FJ, Chern SR, Wu PC, Lee CC, Wang W. Chen CP, et al. Taiwan J Obstet Gynecol. 2010 Dec;49(4):473-80. doi: 10.1016/S1028-4559(10)60100-3. Taiwan J Obstet Gynecol. 2010. PMID: 21199750 Free article.

3

Phenotypic and Molecular Cytogenetic Analysis of a Case of Monosomy 1p36 Syndrome due to Unbalanced Translocation.

Hussen DF, Kamel AK, Mekkawy MK, Ashaat EA, El Ruby MO. Hussen DF, et al. Mol Syndromol. 2020 Dec;11(5-6):284-295. doi: 10.1159/000510428. Epub 2020 Sep 23. Mol Syndromol. 2020. PMID: 33510599 Free PMC article.

4

Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome.

Toshimitsu M, Nagaoka S, Kobori S, Ogawa M, Suzuki F, Kato T, Miyai S, Kawamura R, Inagaki H, Kurahashi H, Murotsuki J. Toshimitsu M, et al. Case Rep Obstet Gynecol. 2019 Oct 2;2019:6753184. doi: 10.1155/2019/6753184. eCollection 2019. Case Rep Obstet Gynecol. 2019. PMID: 31662930 Free PMC article.

5

Electroclinical features of epilepsy monosomy 1p36 syndrome and their implications.

Verrotti A, Greco M, Varriale G, Tamborino A, Savasta S, Carotenuto M, Elia M, Operto F, Margari L, Belcastro V, Selicorni A, Freri E, Matricardi S, Granata T, Ragona F, Capovilla G, Spalice A, Coppola G, Striano P. Verrotti A, et al. Acta Neurol Scand. 2018 Dec;138(6):523-530. doi: 10.1111/ane.13006. Epub 2018 Aug 14. Acta Neurol Scand. 2018. PMID: 30109707

6

Mini-Review: Monosomy 1p36 syndrome: reviewing the correlation between deletion sizes and phenotypes.

Rocha CF, Vasques RB, Santos SR, Paiva CL. Rocha CF, et al. Genet Mol Res. 2016 Feb 22;15(1). doi: 10.4238/gmr.15017942. Genet Mol Res. 2016. PMID: 26910004 Free article. Review.

7

Interstitial deletion 1p36.32 in two brothers with a distinct phenotype--overgrowth, macrocephaly and nearly normal intellectual function.

Di Donato N, Klink B, Hahn G, Schrock E, Hackmann K. Di Donato N, et al. Eur J Med Genet. 2014 Sep;57(9):494-7. doi: 10.1016/j.ejmg.2014.05.004. Epub 2014 May 23. Eur J Med Genet. 2014. PMID: 24862882

8

Accurate, fast and cost-effective diagnostic test for monosomy 1p36 using real-time quantitative PCR.

Cunha Pda S, Pena HB, D'Angelo CS, Koiffmann CP, Rosenfeld JA, Shaffer LG, Stofanko M, Gonçalves-Dornelas H, Pena SD. Cunha Pda S, et al. Dis Markers. 2014;2014:836082. doi: 10.1155/2014/836082. Epub 2014 Apr 15. Dis Markers. 2014. PMID: 24839341 Free PMC article.

9

Monosomy 1p36 - a multifaceted and still enigmatic syndrome: four clinically diverse cases with shared white matter abnormalities.

Õiglane-Shlik E, Puusepp S, Talvik I, Vaher U, Rein R, Tammur P, Reimand T, Teek R, Žilina O, Tomberg T, Õunap K. Õiglane-Shlik E, et al. Eur J Paediatr Neurol. 2014 May;18(3):338-46. doi: 10.1016/j.ejpn.2014.01.008. Epub 2014 Jan 25. Eur J Paediatr Neurol. 2014. PMID: 24529875

10

[Turner syndrome and monosomy 1p36 deletion syndrome misdiagnosed as thyropenia: report of one case].

Meng X, Li Z, Liu T, Wen Z. Meng X, et al. Nan Fang Yi Ke Da Xue Xue Bao. 2013 Dec;33(12):1861-3. Nan Fang Yi Ke Da Xue Xue Bao. 2013. PMID: 24369264 Chinese.

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