PubMed for id: 1641240

Year	Number of Results
1994	2
1999	1
2001	1
2002	1
2003	1
2004	1
2005	1
2011	4
2012	6
2013	4
2014	2
2015	6
2016	2
2017	6
2018	3
2019	7
2020	6
2021	7
2022	6
2023	11
2024	3

1

Loss-of-function of zebrafish cdt1 causes retarded body growth and underdeveloped gonads resembling human Meier-Gorlin syndrome.

He Y, Wang Y, Zhu Y, Lo LJ. He Y, et al. J Zhejiang Univ Sci B. 2023 Nov 15;24(11):1037-1046. doi: 10.1631/jzus.B2300195. J Zhejiang Univ Sci B. 2023. PMID: 37961805 Free PMC article.

2

[Genetic analysis of a child with Meier-Gorlin syndrome due to a variant of ORC6 gene].

Wang L, Wang F, Wang X, Chen L. Wang L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Oct 10;40(10):1292-1295. doi: 10.3760/cma.j.cn511374-20221017-00690. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 37730234 Chinese.

3

The expanding genetic and clinical landscape associated with Meier-Gorlin syndrome.

Nielsen-Dandoroff E, Ruegg MSG, Bicknell LS. Nielsen-Dandoroff E, et al. Eur J Hum Genet. 2023 Aug;31(8):859-868. doi: 10.1038/s41431-023-01359-z. Epub 2023 Apr 14. Eur J Hum Genet. 2023. PMID: 37059840 Free PMC article. Review.

4

Meier-Gorlin Syndrome: Clinical Misdiagnosis, Genetic Testing and Functional Analysis of ORC6 Mutations and the Development of a Prenatal Test.

Nazarenko MS, Viakhireva IV, Skoblov MY, Soloveva EV, Sleptcov AA, Nazarenko LP. Nazarenko MS, et al. Int J Mol Sci. 2022 Aug 17;23(16):9234. doi: 10.3390/ijms23169234. Int J Mol Sci. 2022. PMID: 36012502 Free PMC article.

5

Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome.

McQuaid ME, Ahmed K, Tran S, Rousseau J, Shaheen R, Kernohan KD, Yuki KE, Grover P, Dreseris ES, Ahmed S, Dupuis L, Stimec J, Shago M, Al-Hassnan ZN, Tremblay R, Maass PG, Wilson MD, Grunebaum E, Boycott KM, Boisvert FM, Maddirevula S, Faqeih EA, Almanjomi F, Khan ZU, Alkuraya FS, Campeau PM, Kannu P, Campos EI, Wurtele H. McQuaid ME, et al. JCI Insight. 2022 May 23;7(10):e155648. doi: 10.1172/jci.insight.155648. JCI Insight. 2022. PMID: 35603789 Free PMC article.

6

Meier-Gorlin syndrome with prenatal ultrasound findings and successful growth hormone therapy: Six years follow-up of a rare case.

Vakili R, Mobini M, Hatami F, Vakili S, Valizadeh N. Vakili R, et al. Radiol Case Rep. 2022 Mar 4;17(5):1512-1520. doi: 10.1016/j.radcr.2022.02.028. eCollection 2022 May. Radiol Case Rep. 2022. PMID: 35282325 Free PMC article.

7

Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome.

Zabnenkova V, Shchagina O, Makienko O, Matyushchenko G, Ryzhkova O. Zabnenkova V, et al. Appl Clin Genet. 2022 Jan 6;15:1-10. doi: 10.2147/TACG.S342804. eCollection 2022. Appl Clin Genet. 2022. PMID: 35023948 Free PMC article.

8

Biallelic GINS2 variant p.(Arg114Leu) causes Meier-Gorlin syndrome with craniosynostosis.

Nabais Sá MJ, Miller KA, McQuaid M, Koelling N, Wilkie AOM, Wurtele H, de Brouwer APM, Oliveira J. Nabais Sá MJ, et al. J Med Genet. 2022 Aug;59(8):776-780. doi: 10.1136/jmedgenet-2020-107572. Epub 2021 Aug 5. J Med Genet. 2022. PMID: 34353863 Free PMC article.

9

Prenatal diagnosis of Meier-Gorlin syndrome 7: a case presentation.

Li X, Zhang LZ, Yu L, Long ZL, Lin AY, Gou CY. Li X, et al. BMC Pregnancy Childbirth. 2021 May 17;21(1):381. doi: 10.1186/s12884-021-03868-5. BMC Pregnancy Childbirth. 2021. PMID: 34000999 Free PMC article.

10

MCM complex members MCM3 and MCM7 are associated with a phenotypic spectrum from Meier-Gorlin syndrome to lipodystrophy and adrenal insufficiency.

Knapp KM, Jenkins DE, Sullivan R, Harms FL, von Elsner L, Ockeloen CW, de Munnik S, Bongers EMHF, Murray J, Pachter N, Denecke J, Kutsche K, Bicknell LS. Knapp KM, et al. Eur J Hum Genet. 2021 Jul;29(7):1110-1120. doi: 10.1038/s41431-021-00839-4. Epub 2021 Mar 2. Eur J Hum Genet. 2021. PMID: 33654309 Free PMC article.

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