Zhu S - Search Results

1

Proximal 4p Deletion Syndrome in an Infant With Multiple Systemic Anomalies.

Pang Y, Zeng L, Liang H, Cheng C, Shan L, Wang J, Jiang N, Pi G, Yang L, Chen A, Xiong F, Zhu S. Pang Y, et al. Among authors: zhu s. Mol Genet Genomic Med. 2024 Sep;12(9):e70005. doi: 10.1002/mgg3.70005. Mol Genet Genomic Med. 2024. PMID: 39225318 Free PMC article.

2

Renal-hepatic-pancreatic dysplasia-1 with a novel NPHP3 genotype: a case report and review of the literature.

Zhu H, Zhao ZH, Zhu SY, Xiong F, He LH, Zhang Y, Wang J. Zhu H, et al. BMC Pediatr. 2022 Oct 18;22(1):603. doi: 10.1186/s12887-022-03659-7. BMC Pediatr. 2022. PMID: 36253741 Free PMC article. Review.

3

The RRAS2 pathogenic variant (c.67G>T; p. Gly23Cys) produces Noonan syndrome with embryonal rhabdomyosarcoma.

Zeng L, Wang J, Zhu H, Huang Y, Deng Y, Wei P, Nie J, Tang B, Chen A, Zhu S. Zeng L, et al. Among authors: zhu s, zhu h. Mol Genet Genomic Med. 2024 Jan;12(1):e2313. doi: 10.1002/mgg3.2313. Epub 2023 Nov 9. Mol Genet Genomic Med. 2024. PMID: 37942564 Free PMC article.

4

Vulto-van Silfhout-de Vries syndrome caused by de novo variants of DEAF1 gene: a case report and literature review.

Zhu H, Zhu S, Jiang Q, Pang Y, Huang Y, Chen Y, Hou T, Deng W, Liu X, Zeng L, Chen A, Wang J, Luo Z. Zhu H, et al. Among authors: zhu s. Front Neurol. 2023 Nov 24;14:1251467. doi: 10.3389/fneur.2023.1251467. eCollection 2023. Front Neurol. 2023. PMID: 38073621 Free PMC article.

5

Genetic analysis of a pedigree with MECP2 duplication syndrome in China.

Zeng L, Zhu H, Wang J, Wang Q, Pang Y, Luo Z, Chen A, Qin S, Zhu S. Zeng L, et al. Among authors: zhu s, zhu h. BMC Med Genomics. 2024 Feb 19;17(1):54. doi: 10.1186/s12920-024-01831-9. BMC Med Genomics. 2024. PMID: 38373942 Free PMC article.

6

Genotype characterization of tetrahydrobiopterin deficiency in two Tibetan children.

Zhu S, Hu Q, Yang Y, Zhu H, Wang J, Luo Z, Ou M, Chen A, Huang Y, Xiong F, Zhou J, Liu J, Lei X, Zeng L. Zhu S, et al. Among authors: zhu h. Heliyon. 2024 Feb 24;10(5):e27050. doi: 10.1016/j.heliyon.2024.e27050. eCollection 2024 Mar 15. Heliyon. 2024. PMID: 38434370 Free PMC article.

7

Dual diagnosis of microcephalic osteosplastic primary dwarfism type II and benign familial infantile seizure type 2: a case report.

Zhu S, Wang J, Zhu H, Wang Q, Tang B, Xiong F, Luo Z, Chen A, Wang X, Leng X, Zeng L. Zhu S, et al. Among authors: zhu h. Clin Dysmorphol. 2024 Apr 1;33(2):83-86. doi: 10.1097/MCD.0000000000000493. Epub 2024 Feb 6. Clin Dysmorphol. 2024. PMID: 38441202 Free PMC article. No abstract available.

8

Acute Necrotizing Encephalopathy Associated with SARS-CoV-2 Infection in Children.

Zhu H, Zhu S, Wang Q, Wang L, Jiang Q, Hu Y, Huang Y, Zeng L, Luo Z. Zhu H, et al. Among authors: zhu s. Ann Indian Acad Neurol. 2024 Mar-Apr;27(2):222-225. doi: 10.4103/aian.aian_912_23. Epub 2024 Apr 5. Ann Indian Acad Neurol. 2024. PMID: 38751924 Free PMC article. No abstract available.

9

Bmal1 regulates female reproduction in mice via the hypothalamic-pituitary-ovarian axis.

Zhang A, Li S, Huang L, Jiang Y, Chen Y, Zhu S, Xiong F, Luo Z, Ou M, Ying J, Wang S, Mu D, Qu Y. Zhang A, et al. Among authors: zhu s. FASEB J. 2024 Jul 15;38(13):e23744. doi: 10.1096/fj.202400391R. FASEB J. 2024. PMID: 38885031

10

Genetic Analysis of De Novo Variants in KMT2A mixed-lineage leukemia Identified in a Family of Wiedermann-Steiner Syndromes.

Cao M, Dan T, Nie X, Tang B, Zeng L, Pi G, Chen A, Luo H, Zhu S. Cao M, et al. Among authors: zhu s. Ann Indian Acad Neurol. 2024 Jul 1;27(4):455-457. doi: 10.4103/aian.aian_108_24. Epub 2024 Aug 8. Ann Indian Acad Neurol. 2024. PMID: 39113367 Free PMC article. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

17,757 results

Search Page

Filters