These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
160 related articles for article (PubMed ID: 37147621)
1. Molecular genetic screening of full-term small for gestational age. Zhang S; Zhou L; Zhang L; Wang Y; Wang H BMC Pediatr; 2023 May; 23(1):217. PubMed ID: 37147621 [TBL] [Abstract][Full Text] [Related]
2. Molecular Genetic Screening of Neonatal Intensive Care Units: Hyperbilirubinemia as an Example. Yang Y; Wang Y; Zhou L; Long W; Yu B; Wang H Appl Clin Genet; 2022; 15():39-48. PubMed ID: 35611242 [TBL] [Abstract][Full Text] [Related]
3. Applying targeted next generation sequencing to dried blood spot specimens from suspicious cases identified by tandem mass spectrometry-based newborn screening. Qian J; Wang X; Liu J; Zhong J; Le Y; Melchior Tellier LCA; Liu C; Jiang P; Gao R; Wang Y J Pediatr Endocrinol Metab; 2017 Aug; 30(9):979-988. PubMed ID: 28771436 [TBL] [Abstract][Full Text] [Related]
4. Pilot study of newborn screening of inborn error of metabolism using tandem mass spectrometry in Malaysia: outcome and challenges. Yunus ZM; Rahman SA; Choy YS; Keng WT; Ngu LH J Pediatr Endocrinol Metab; 2016 Sep; 29(9):1031-9. PubMed ID: 27544719 [TBL] [Abstract][Full Text] [Related]
5. NeoSeq: a new method of genomic sequencing for newborn screening. Wang H; Yang Y; Zhou L; Wang Y; Long W; Yu B Orphanet J Rare Dis; 2021 Nov; 16(1):481. PubMed ID: 34794485 [TBL] [Abstract][Full Text] [Related]
6. Diagnosis and therapeutic monitoring of inborn errors of metabolism in 100,077 newborns from Jining city in China. Yang CJ; Wei N; Li M; Xie K; Li JQ; Huang CG; Xiao YS; Liu WH; Chen XG BMC Pediatr; 2018 Mar; 18(1):110. PubMed ID: 29534692 [TBL] [Abstract][Full Text] [Related]
7. A multicenter prospective study of next-generation sequencing-based newborn screening for monogenic genetic diseases in China. Yang RL; Qian GL; Wu DW; Miao JK; Yang X; Wu BQ; Yan YQ; Li HB; Mao XM; He J; Shen H; Zou H; Xue SY; Li XZ; Niu TT; Xiao R; Zhao ZY World J Pediatr; 2023 Jul; 19(7):663-673. PubMed ID: 36847978 [TBL] [Abstract][Full Text] [Related]
8. 3-Methylcrotonyl-CoA carboxylase deficiency newborn screening in a population of 536,008: is routine screening necessary? Wang H; Liu S; Wang B; Yang Y; Yu B; Wang L; Wang T J Pediatr Endocrinol Metab; 2019 Dec; 32(12):1321-1326. PubMed ID: 31730530 [TBL] [Abstract][Full Text] [Related]
10. A comprehensive multiplex PCR based exome-sequencing assay for rapid bloodspot confirmation of inborn errors of metabolism. Wang W; Yang J; Xue J; Mu W; Zhang X; Wu W; Xu M; Gong Y; Liu Y; Zhang Y; Xie X; Gu W; Bai J; Cram DS BMC Med Genet; 2019 Jan; 20(1):3. PubMed ID: 30612563 [TBL] [Abstract][Full Text] [Related]
11. Inborn errors of metabolism detectable by tandem mass spectrometry in Beijing. Yang N; Gong LF; Zhao JQ; Yang HH; Ma ZJ; Liu W; Wan ZH; Kong YY J Pediatr Endocrinol Metab; 2020 May; 33(5):639-645. PubMed ID: 32304307 [TBL] [Abstract][Full Text] [Related]
12. Fetal growth restriction and intra-uterine growth restriction: guidelines for clinical practice from the French College of Gynaecologists and Obstetricians. Vayssière C; Sentilhes L; Ego A; Bernard C; Cambourieu D; Flamant C; Gascoin G; Gaudineau A; Grangé G; Houfflin-Debarge V; Langer B; Malan V; Marcorelles P; Nizard J; Perrotin F; Salomon L; Senat MV; Serry A; Tessier V; Truffert P; Tsatsaris V; Arnaud C; Carbonne B Eur J Obstet Gynecol Reprod Biol; 2015 Oct; 193():10-8. PubMed ID: 26207980 [TBL] [Abstract][Full Text] [Related]
13. Application of Next-Generation Sequencing Following Tandem Mass Spectrometry to Expand Newborn Screening for Inborn Errors of Metabolism: A Multicenter Study. Yang Y; Wang L; Wang B; Liu S; Yu B; Wang T Front Genet; 2019; 10():86. PubMed ID: 30838026 [TBL] [Abstract][Full Text] [Related]
14. [Small for gestational age newborns--definition, etiology and neonatal treatment]. Slancheva B; Mumdzhiev H Akush Ginekol (Sofiia); 2013; 52(2):25-32. PubMed ID: 23807977 [TBL] [Abstract][Full Text] [Related]
15. Thyroid Hormone Function in Small for Gestational Age Term Newborns. Kaluarachchi DC; Nicksic VB; Allen DB; Eickhoff JC; Baker MW; Kling PJ J Pediatr; 2021 Nov; 238():181-186.e3. PubMed ID: 34214586 [TBL] [Abstract][Full Text] [Related]
16. Sequencing from dried blood spots in infants with "false positive" newborn screen for MCAD deficiency. McCandless SE; Chandrasekar R; Linard S; Kikano S; Rice L Mol Genet Metab; 2013 Jan; 108(1):51-5. PubMed ID: 23151387 [TBL] [Abstract][Full Text] [Related]
17. A retrospective analysis of MS/MS screening for IEM in high-risk areas. He X; Kuang J; Lai J; Huang J; Wang Y; Lan G; Xie Y; Shi X BMC Med Genomics; 2023 Mar; 16(1):57. PubMed ID: 36927542 [TBL] [Abstract][Full Text] [Related]
18. Association Analysis of Gene Sequencing by NeoSeq Combined with Tandem Mass Spectrum and Four Neonatal Diseases. Xue S; Zhu J; Zhang H; Han L; Yang R; Dai P; Ding G Clin Lab; 2023 Sep; 69(9):. PubMed ID: 37702680 [TBL] [Abstract][Full Text] [Related]
19. Subchromosomal anomalies in small for gestational-age fetuses and newborns. Ma Y; Pei Y; Yin C; Jiang Y; Wang J; Li X; Li L; Kagan KO; Wu Q Arch Gynecol Obstet; 2019 Sep; 300(3):633-639. PubMed ID: 31273521 [TBL] [Abstract][Full Text] [Related]
20. Diagnosis of immunodeficiency caused by a purine nucleoside phosphorylase defect by using tandem mass spectrometry on dried blood spots. la Marca G; Canessa C; Giocaliere E; Romano F; Malvagia S; Funghini S; Moriondo M; Valleriani C; Lippi F; Ombrone D; Della Bona ML; Speckmann C; Borte S; Brodszki N; Gennery AR; Weinacht K; Celmeli F; Pagel J; de Martino M; Guerrini R; Wittkowski H; Santisteban I; Bali P; Ikinciogullari A; Hershfield M; Notarangelo LD; Resti M; Azzari C J Allergy Clin Immunol; 2014 Jul; 134(1):155-9. PubMed ID: 24767876 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]