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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1997 1
2000 1
2001 2
2002 2
2003 2
2004 3
2005 4
2006 2
2007 1
2008 2
2009 3
2010 4
2011 10
2012 4
2013 4
2014 5
2015 3
2016 1
2017 5
2018 3
2019 1
2020 4
2023 1

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61 results

Results by year

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Page 1
Family history: the three-generation pedigree.
Wattendorf DJ, Hadley DW. Wattendorf DJ, et al. Among authors: hadley dw. Am Fam Physician. 2005 Aug 1;72(3):441-8. Am Fam Physician. 2005. PMID: 16100858 Free article. Review.
Genetic testing in Parkinson's disease.
McInerney-Leo A, Hadley DW, Gwinn-Hardy K, Hardy J. McInerney-Leo A, et al. Among authors: hadley dw. Mov Disord. 2005 Jan;20(1):1-10. doi: 10.1002/mds.20316. Mov Disord. 2005. PMID: 15503301 Review.
The Human Genome Project: an update.
Peters KF, Menaker TJ, Wilson PL, Hadley DW. Peters KF, et al. Among authors: hadley dw. Cancer Nurs. 2001 Aug;24(4):287-92; quiz 292-3. doi: 10.1097/00002820-200108000-00007. Cancer Nurs. 2001. PMID: 11502037 Review.
An approach to the identification of anomalies and etiologies in neonates with identified or suspected VACTERL (vertebral defects, anal atresia, tracheo-esophageal fistula with esophageal atresia, cardiac anomalies, renal anomalies, and limb anomalies) association.
Solomon BD, Baker LA, Bear KA, Cunningham BK, Giampietro PF, Hadigan C, Hadley DW, Harrison S, Levitt MA, Niforatos N, Paul SM, Raggio C, Reutter H, Warren-Mora N. Solomon BD, et al. Among authors: hadley dw. J Pediatr. 2014 Mar;164(3):451-7.e1. doi: 10.1016/j.jpeds.2013.10.086. Epub 2013 Dec 12. J Pediatr. 2014. PMID: 24332453 Free PMC article. Review. No abstract available.
SIX3 deletions and incomplete penetrance in families affected by holoprosencephaly.
Stokes B, Berger SI, Hall BA, Weiss K, Martinez AF, Hadley DW, Murdock DR, Ramanathan S, Clark RD, Roessler E, Kruszka P, Muenke M. Stokes B, et al. Among authors: hadley dw. Congenit Anom (Kyoto). 2018 Jan;58(1):29-32. doi: 10.1111/cga.12234. Epub 2017 Aug 1. Congenit Anom (Kyoto). 2018. PMID: 28670735 Free PMC article.
Muenke syndrome: An international multicenter natural history study.
Kruszka P, Addissie YA, Yarnell CM, Hadley DW, Guillen Sacoto MJ, Platte P, Paelecke Y, Collmann H, Snow N, Schweitzer T, Boyadjiev SA, Aravidis C, Hall SE, Mulliken JB, Roscioli T, Muenke M. Kruszka P, et al. Among authors: hadley dw. Am J Med Genet A. 2016 Apr;170A(4):918-29. doi: 10.1002/ajmg.a.37528. Epub 2016 Jan 6. Am J Med Genet A. 2016. PMID: 26740388
61 results