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Items: 6

1.
2.

Whole exome sequencing identifies a pathogenic mutation in WFS1 in two large Chinese families with autosomal dominant all-frequency hearing loss and prenatal counseling.

Cheng H, Zhang Q, Wang W, Meng Q, Wang F, Liu M, Mao J, Shi Y, Wang W, Li H.

Int J Pediatr Otorhinolaryngol. 2018 Mar;106:113-119. doi: 10.1016/j.ijporl.2018.01.005. Epub 2018 Jan 31.

PMID:
29447883
3.

Efficiency of mild ovarian stimulation with clomiphene on poor ovarian responders during IVF\ICSI procedures: a meta-analysis.

Song D, Shi Y, Zhong Y, Meng Q, Hou S, Li H.

Eur J Obstet Gynecol Reprod Biol. 2016 Sep;204:36-43. doi: 10.1016/j.ejogrb.2016.07.498. Epub 2016 Aug 3. Review.

PMID:
27521596
4.

Identification of small segmental translocations in patients with repeated implantation failure and recurrent miscarriage using next generation sequencing after in vitro fertilization/intracytoplasmic sperm injection.

Ou J, Wang W, Feng T, Liao L, Meng Q, Zou Q, Ding J, Zheng A, Duan C, Li P, Liu Q, Lin C, Li H.

Mol Cytogenet. 2015 Dec 30;8:105. doi: 10.1186/s13039-015-0207-7. eCollection 2015.

5.

Early acetabular cartilage degeneration in a rabbit model of developmental dysplasia of the hip.

Zhang X, Meng Q, Ma R, Chen G, Cheng L, Shen J.

Int J Clin Exp Med. 2015 Aug 15;8(8):14505-12. eCollection 2015.

6.

[Rapid identification of cortex dictamni pieces and its counterfeit alangium Chinense by spectral imaging method].

Zhao J, Pang Q, Ma J, Liu C, Wang L, Meng Q.

Zhongguo Zhong Yao Za Zhi. 2010 Jul;35(13):1696-8. Chinese.

PMID:
20862959

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