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

Year Number of Results
1984 1
1986 2
1987 3
1988 4
1989 2
1990 1
1993 3
1997 1
2000 1
2002 1
2005 1
2007 2
2008 1
2009 1
2010 1
2011 1
2012 2
2013 2
2014 1
2024 0

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29 results

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Page 1
Identification and evaluation of mental retardation.
Daily DK, Ardinger HH, Holmes GE. Daily DK, et al. Among authors: ardinger hh. Am Fam Physician. 2000 Feb 15;61(4):1059-67, 1070. Am Fam Physician. 2000. PMID: 10706158 Free article. Review.
CDKN1C mutations and genital anomalies.
Welsh HI, Stockley TL, Parkinson N, Ardinger HH. Welsh HI, et al. Among authors: ardinger hh. Am J Med Genet A. 2012 Jan;158A(1):265. doi: 10.1002/ajmg.a.34388. Epub 2011 Dec 2. Am J Med Genet A. 2012. PMID: 22140035 No abstract available.
Verification of the fetal valproate syndrome phenotype.
Ardinger HH, Atkin JF, Blackston RD, Elsas LJ, Clarren SK, Livingstone S, Flannery DB, Pellock JM, Harrod MJ, Lammer EJ, et al. Ardinger HH, et al. Am J Med Genet. 1988 Jan;29(1):171-85. doi: 10.1002/ajmg.1320290123. Am J Med Genet. 1988. PMID: 3125743 Review.
Dominantly inherited dilated cardiomyopathy.
Gardner RJ, Hanson JW, Ionasescu VV, Ardinger HH, Skorton DJ, Mahoney LT, Hart MN, Rose EF, Smith WL, Florentine MS, et al. Gardner RJ, et al. Among authors: ardinger hh. Am J Med Genet. 1987 May;27(1):61-73. doi: 10.1002/ajmg.1320270108. Am J Med Genet. 1987. PMID: 3605207
Further delineation of Weaver syndrome.
Ardinger HH, Hanson JW, Harrod MJ, Cohen MM Jr, Tibbles JA, Welch JP, Young-Wee T, Sommer A, Goldberg R, Shprintzen RJ, et al. Ardinger HH, et al. J Pediatr. 1986 Feb;108(2):228-35. doi: 10.1016/s0022-3476(86)80988-x. J Pediatr. 1986. PMID: 2418189
Maternal serum screening and 22q11.2 deletion syndrome.
Begleiter ML, Lund MM, Atherton AM, Buchholz JD, Ardinger HH. Begleiter ML, et al. Among authors: ardinger hh. Am J Med Genet A. 2007 Feb 15;143(4):410-1. doi: 10.1002/ajmg.a.31616. Am J Med Genet A. 2007. PMID: 17230492 No abstract available.
29 results