PubMed for id: 321954

Year	Number of Results
1981	2
1985	2
1990	1
1992	2
1993	1
1995	2
1997	1
1998	2
2000	1
2002	3
2004	1
2007	1
2008	3
2009	2
2010	3
2011	3
2012	2
2013	1
2015	3
2016	26
2017	68
2018	86
2019	72
2020	79
2021	83
2022	85
2023	59

1

Prenatal diagnosis and postnatal followup of partial trisomy 13q and partial monosomy 10p: a case report and review of the literature.

Wei Y, Gao X, Yan L, Xu F, Li P, Zhao Y. Wei Y, et al. Case Rep Genet. 2012;2012:821347. doi: 10.1155/2012/821347. Epub 2012 Oct 23. Case Rep Genet. 2012. PMID: 23133763 Free PMC article.

2

Combined partial trisomy 11q and partial monosomy 10p in a 19-year-old female patient: phenotypic and genotypic findings.

Hagen A, Bigl A, Wand D, Klopocki E, Heller R, Siekmeyer M, Siekmeyer W, Kiess W, Merkenschlager A. Hagen A, et al. Am J Med Genet A. 2011 Dec;155A(12):3075-81. doi: 10.1002/ajmg.a.34300. Epub 2011 Nov 3. Am J Med Genet A. 2011. PMID: 22052712

3

10p12.1 deletion: HDR phenotype without DGS2 features.

Benetti E, Murer L, Bordugo A, Andreetta B, Artifoni L. Benetti E, et al. Exp Mol Pathol. 2009 Feb;86(1):74-6. doi: 10.1016/j.yexmp.2008.10.003. Epub 2008 Oct 31. Exp Mol Pathol. 2009. PMID: 19022243

4

Chromosome 10p deletion in a patient with hypoparathyroidism, severe mental retardation, autism and basal ganglia calcifications.

Verri A, Maraschio P, Devriendt K, Uggetti C, Spadoni E, Haeusler E, Federico A. Verri A, et al. Ann Genet. 2004 Jul-Sep;47(3):281-7. doi: 10.1016/j.anngen.2004.03.001. Ann Genet. 2004. PMID: 15337474

5

Molecular cytogenetic characterization of a 10p14 deletion that includes the DGS2 region in a patient with multiple anomalies.

Skrypnyk C, Goecke TO, Majewski F, Bartsch O. Skrypnyk C, et al. Am J Med Genet. 2002 Nov 22;113(2):207-12. doi: 10.1002/ajmg.10764. Am J Med Genet. 2002. PMID: 12407714

6

Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p.

Lichtner P, Attié-Bitach T, Schuffenhauer S, Henwood J, Bouvagnet P, Scambler PJ, Meitinger T, Vekemans M. Lichtner P, et al. J Mol Med (Berl). 2002 Jul;80(7):431-42. doi: 10.1007/s00109-002-0331-9. Epub 2002 Apr 4. J Mol Med (Berl). 2002. PMID: 12110949

7

Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2).

Schuffenhauer S, Lichtner P, Peykar-Derakhshandeh P, Murken J, Haas OA, Back E, Wolff G, Zabel B, Barisic I, Rauch A, Borochowitz Z, Dallapiccola B, Ross M, Meitinger T. Schuffenhauer S, et al. Eur J Hum Genet. 1998 May-Jun;6(3):213-25. doi: 10.1038/sj.ejhg.5200183. Eur J Hum Genet. 1998. PMID: 9781025

8

MRI findings in a patient with partial monosomy 10p.

Sunada F, Rash FC, Tam DA. Sunada F, et al. J Med Genet. 1998 Feb;35(2):159-61. doi: 10.1136/jmg.35.2.159. J Med Genet. 1998. PMID: 9507399 Free PMC article.

9

DiGeorge syndrome and partial monosomy 10p: case report and review.

Schuffenhauer S, Seidel H, Oechsler H, Belohradsky B, Bernsau U, Murken J, Meitinger T. Schuffenhauer S, et al. Ann Genet. 1995;38(3):162-7. Ann Genet. 1995. PMID: 8540688 Review.

10

A case of de novo translocation 7; 10 and the duplication 7p, deletion 10p phenotype.

Park JP, McDermet MK, Moeschler JB, Wurster-Hill DH. Park JP, et al. Ann Genet. 1993;36(4):217-20. Ann Genet. 1993. PMID: 8166428

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