Tan WH - Search Results

1

Prenatal imaging throughout gestation in Beckwith-Wiedemann syndrome.

Shieh HF, Estroff JA, Barnewolt CE, Zurakowski D, Tan WH, Buchmiller TL. Shieh HF, et al. Among authors: tan wh. Prenat Diagn. 2019 Aug;39(9):792-795. doi: 10.1002/pd.5440. Epub 2019 Mar 18. Prenat Diagn. 2019. PMID: 30784096

2

Genetic diagnoses and associated anomalies in fetuses prenatally diagnosed with esophageal atresia.

Rohanizadegan M, Tracy S, Galarreta CI, Poorvu T, Buchmiller TL, Bird LM, Estroff JA, Tan WH. Rohanizadegan M, et al. Among authors: tan wh. Am J Med Genet A. 2020 Aug;182(8):1890-1895. doi: 10.1002/ajmg.a.61639. Epub 2020 Jun 23. Am J Med Genet A. 2020. PMID: 32573094

3

Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletions.

Verscaj CP, Velez-Bartolomei F, Bodle E, Chan K, Lyons MJ, Thorson W, Tan WH, Rodig N, Graham JM Jr, Peron A, Quintero-Rivera F, Zackai EH, Thomas MA, Stevens CA, Adam MP, Bird LM, Jones MC, Matalon DR. Verscaj CP, et al. Among authors: tan wh. Prenat Diagn. 2024 Feb;44(2):237-246. doi: 10.1002/pd.6424. Epub 2023 Aug 26. Prenat Diagn. 2024. PMID: 37632214 Review.

4

Healthcare burden among individuals with Angelman syndrome: Findings from the Angelman Syndrome Natural History Study.

Khan N, Cabo R, Tan WH, Tayag R, Bird LM. Khan N, et al. Among authors: tan wh. Mol Genet Genomic Med. 2019 Jul;7(7):e00734. doi: 10.1002/mgg3.734. Epub 2019 May 14. Mol Genet Genomic Med. 2019. PMID: 31090212 Free PMC article.

5

Clinical Characterization of Epilepsy in Children With Angelman Syndrome.

Cassater D, Bustamante M, Sach-Peltason L, Rotenberg A, Nespeca M, Tan WH, Bird LM, Hipp JF. Cassater D, et al. Among authors: tan wh. Pediatr Neurol. 2021 Nov;124:42-50. doi: 10.1016/j.pediatrneurol.2021.08.007. Epub 2021 Aug 31. Pediatr Neurol. 2021. PMID: 34536900 Free PMC article. Clinical Trial.

6

PTEN hamartoma tumour syndrome: early tumour development in children.

Smpokou P, Fox VL, Tan WH. Smpokou P, et al. Among authors: tan wh. Arch Dis Child. 2015 Jan;100(1):34-7. doi: 10.1136/archdischild-2014-305997. Epub 2014 Aug 11. Arch Dis Child. 2015. PMID: 25114091

7

Infant mortality: the contribution of genetic disorders.

Wojcik MH, Schwartz TS, Thiele KE, Paterson H, Stadelmaier R, Mullen TE, VanNoy GE, Genetti CA, Madden JA, Gubbels CS, Yu TW, Tan WH, Agrawal PB. Wojcik MH, et al. Among authors: tan wh. J Perinatol. 2019 Dec;39(12):1611-1619. doi: 10.1038/s41372-019-0451-5. Epub 2019 Aug 8. J Perinatol. 2019. PMID: 31395954 Free PMC article.

8

Neurodevelopmental profile of siblings with Angelman syndrome due to pathogenic UBE3A variants.

Sadhwani A, Willen JM, Miller H, Barbieri-Welge R, Horowitz LT, Noll LM, Peters S, Hundley R, Bird LM, Tan WH. Sadhwani A, et al. Among authors: tan wh. J Intellect Disabil Res. 2020 Mar;64(3):246-250. doi: 10.1111/jir.12700. Epub 2019 Dec 19. J Intellect Disabil Res. 2020. PMID: 31854050 Free PMC article.

9

Polymicrogyria is Associated With Pathogenic Variants in PTEN.

Shao DD, Achkar CM, Lai A, Srivastava S, Doan RN, Rodan LH, Chen AY; Brain Development Study Group; Poduri A, Yang E, Walsh CA. Shao DD, et al. Ann Neurol. 2020 Dec;88(6):1153-1164. doi: 10.1002/ana.25904. Epub 2020 Oct 8. Ann Neurol. 2020. PMID: 32959437 Free PMC article.

10

Cockayne syndrome: the developing phenotype.

Tan WH, Baris H, Robson CD, Kimonis VE. Tan WH, et al. Am J Med Genet A. 2005 Jun 1;135(2):214-6. doi: 10.1002/ajmg.a.30731. Am J Med Genet A. 2005. PMID: 15887300

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