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

Year Number of Results
1981 1
1982 2
1985 3
1987 5
1988 3
1990 1
1993 3
1995 1
1996 1
1998 1
1999 2
2001 1
2002 1
2004 1
2007 1
2011 2
2012 1
2013 1
2021 1
2022 1
2024 0

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31 results

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Page 1
Clinical and behavioral characteristics in FG syndrome.
Graham JM Jr, Superneau D, Rogers RC, Corning K, Schwartz CE, Dykens EM. Graham JM Jr, et al. Among authors: superneau d. Am J Med Genet. 1999 Aug 27;85(5):470-5. Am J Med Genet. 1999. PMID: 10405444
Genome sequencing as a first-line diagnostic test for hospitalized infants.
Bowling KM, Thompson ML, Finnila CR, Hiatt SM, Latner DR, Amaral MD, Lawlor JMJ, East KM, Cochran ME, Greve V, Kelley WV, Gray DE, Felker SA, Meddaugh H, Cannon A, Luedecke A, Jackson KE, Hendon LG, Janani HM, Johnston M, Merin LA, Deans SL, Tuura C, Williams H, Laborde K, Neu MB, Patrick-Esteve J, Hurst ACE, Kandasamy J, Carlo W, Brothers KB, Kirmse BM, Savich R, Superneau D, Spedale SB, Knight SJ, Barsh GS, Korf BR, Cooper GM. Bowling KM, et al. Among authors: superneau d. Genet Med. 2022 Apr;24(4):851-861. doi: 10.1016/j.gim.2021.11.020. Epub 2021 Nov 27. Genet Med. 2022. PMID: 34930662 Free PMC article.
Meier-Gorlin syndrome: report of eight additional cases and review.
Bongers EM, Opitz JM, Fryer A, Sarda P, Hennekam RC, Hall BD, Superneau DW, Harbison M, Poss A, van Bokhoven H, Hamel BC, Knoers NV. Bongers EM, et al. Among authors: superneau dw. Am J Med Genet. 2001 Aug 1;102(2):115-24. doi: 10.1002/ajmg.1452. Am J Med Genet. 2001. PMID: 11477602 Review.
Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?
Bohring A, Silengo M, Lerone M, Superneau DW, Spaich C, Braddock SR, Poss A, Opitz JM. Bohring A, et al. Among authors: superneau dw. Am J Med Genet. 1999 Aug 27;85(5):438-46. doi: 10.1002/(sici)1096-8628(19990827)85:5<438::aid-ajmg2>3.0.co;2-a. Am J Med Genet. 1999. PMID: 10405439 Review.
Angiomas and von Recklinghausen neurofibromatosis.
Wertelecki W, Superneau DW, Forehand LW, Hoff CJ. Wertelecki W, et al. Among authors: superneau dw. Neurofibromatosis. 1988;1(3):137-45. Neurofibromatosis. 1988. PMID: 3152460
Myopathy in Marinesco-Sjogren syndrome.
Superneau DW, Wertelecki W, Zellweger H, Bastian F. Superneau DW, et al. Eur Neurol. 1987;26(1):8-16. doi: 10.1159/000116305. Eur Neurol. 1987. PMID: 3469098
Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome.
Guernsey DL, Matsuoka M, Jiang H, Evans S, Macgillivray C, Nightingale M, Perry S, Ferguson M, LeBlanc M, Paquette J, Patry L, Rideout AL, Thomas A, Orr A, McMaster CR, Michaud JL, Deal C, Langlois S, Superneau DW, Parkash S, Ludman M, Skidmore DL, Samuels ME. Guernsey DL, et al. Among authors: superneau dw. Nat Genet. 2011 Feb 27;43(4):360-4. doi: 10.1038/ng.777. Nat Genet. 2011. PMID: 21358631
Fertility and the cri du chat syndrome.
Martínez JE, Tuck-Muller CM, Superneau D, Wertelecki W. Martínez JE, et al. Among authors: superneau d. Clin Genet. 1993 Apr;43(4):212-4. doi: 10.1111/j.1399-0004.1993.tb04467.x. Clin Genet. 1993. PMID: 8330455
31 results