PubMed for id: 162917

Year	Number of Results
1984	1
1988	2
1991	2
1992	4
1993	3
1994	4
1995	2
1996	3
1997	7
1998	13
1999	7
2000	6
2001	9
2002	2
2003	7
2004	4
2005	11
2006	9
2007	8
2008	12
2009	18
2010	21
2011	30
2012	33
2013	26
2014	21
2015	27
2016	31
2017	21
2018	27
2019	33
2020	28
2021	27
2022	32
2023	35
2024	8

1

A Case of Simpson-Golabi-Behmel Syndrome Presenting with Cutaneous Findings.

Mullins T, Russell A, Johnston C. Mullins T, et al. HCA Healthc J Med. 2020 Dec 29;1(6):481-483. doi: 10.36518/2689-0216.1058. eCollection 2020. HCA Healthc J Med. 2020. PMID: 37427042 Free PMC article.

2

Effects of allicin on human Simpson-Golabi-Behmel syndrome cells in mediating browning phenotype.

Ali U, Wabitsch M, Tews D, Colitti M. Ali U, et al. Front Endocrinol (Lausanne). 2023 Mar 1;14:1141303. doi: 10.3389/fendo.2023.1141303. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 36936145 Free PMC article.

3

Prenatal diagnosis of Simpson-Golabi-Behmel syndrome type 1 with an 814 kb Xq26.2 deletion with the initial presentation of a thick nuchal fold.

Peng HH, Yu CJ, Chen YC, Hsu CC, Chang SD, Chueh HY, Chang YL, Cheng PJ, Lee YC. Peng HH, et al. Taiwan J Obstet Gynecol. 2023 Jan;62(1):163-166. doi: 10.1016/j.tjog.2022.06.019. Taiwan J Obstet Gynecol. 2023. PMID: 36720533 Free article.

4

Novel GPC3 Gene Mutation in Simpson-Golabi-Behmel Syndrome with Endocrine Anomalies: A Case Report.

Bu W, Zhu M, Li S, Liu H, Liu X. Bu W, et al. Balkan J Med Genet. 2022 Jun 5;24(2):95-98. doi: 10.2478/bjmg-2021-0024. eCollection 2021 Nov. Balkan J Med Genet. 2022. PMID: 36249515 Free PMC article.

5

SIMPSON-GOLABI-BEHMEL syndrome type 1: How placental immunohistochemistry can rapidly Predict the diagnosis.

Fiandrino G, Arossa A, Ghirardello S, Kalantari S, Rossi C, Bonasoni MP, Cesari S, Rizzuti T, Giorgio E, Bassanese F, Scatigno AL, Meroni A, Melito C, Feltri M, Longo S, Figar TA, Andorno A, Gelli MC, Bertozzi M, Spinillo A, Riccipetitoni G, Valente EM, Paulli M, Sirchia F. Fiandrino G, et al. Placenta. 2022 Aug;126:119-124. doi: 10.1016/j.placenta.2022.06.011. Epub 2022 Jun 30. Placenta. 2022. PMID: 35796063

6

Precocious puberty in a case of Simpson-Golabi-Behmel syndrome with a de novo 240-kb deletion including GPC3.

Watanabe K, Noguchi A, Takahashi I, Yamada M, Suzuki H, Takenouchi T, Kosaki K, Takahashi T. Watanabe K, et al. Hum Genome Var. 2022 Jun 9;9(1):23. doi: 10.1038/s41439-022-00196-8. Hum Genome Var. 2022. PMID: 35680838 Free PMC article.

7

Transcriptomic analysis of Simpson Golabi Behmel syndrome cells during differentiation exhibit BAT-like function.

Colitti M, Ali U, Wabitsch M, Tews D. Colitti M, et al. Tissue Cell. 2022 Aug;77:101822. doi: 10.1016/j.tice.2022.101822. Epub 2022 May 18. Tissue Cell. 2022. PMID: 35623306

8

A prenatal case of Simpson-Golabi-Behmel syndrome type 1 with a 0.26-Mb deletion fragment at Xq26.2 inherited from mother: Case report.

Sha J, Tan F, Liu Y, Xu Z, Wang X, Zhai J. Sha J, et al. Medicine (Baltimore). 2022 Apr 22;101(16):e29222. doi: 10.1097/MD.0000000000029222. Medicine (Baltimore). 2022. PMID: 35482990 Free PMC article.

9

Simpson-Golabi-Behmel syndrome in one of the Dichorionic-diamniotic twin: a case report and literature review.

Guo Y, Zhang H, Fan L, Chen J, Zhang X, Yang H, Sun Y. Guo Y, et al. BMC Pregnancy Childbirth. 2022 Jan 17;22(1):42. doi: 10.1186/s12884-021-04309-z. BMC Pregnancy Childbirth. 2022. PMID: 35038998 Free PMC article. Review.

10

Prenatal case of Simpson-Golabi-Behmel syndrome with a de novo 370Kb-sized microdeletion of Xq26.2 compassing partial GPC3 gene and review.

Liu J, Liu Q, Yang S, Ma N, Pang J, Peng Y, Xi H, Jia Z, Luo Y, Jiang M, Teng Y, Yu W, Li Z, Wang H. Liu J, et al. Mol Genet Genomic Med. 2021 Aug;9(8):e1750. doi: 10.1002/mgg3.1750. Epub 2021 Jul 22. Mol Genet Genomic Med. 2021. PMID: 34293831 Free PMC article. Review.

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