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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
2023 0
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Search Results

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.
Linkage localization of Börjeson-Forssman-Lehmann syndrome.
Mathews KD, Ardinger HH, Nishimura DY, Buetow KH, Murray JC, Bartley JA. Mathews KD, et al. Among authors: ardinger hh. Am J Med Genet. 1989 Dec;34(4):470-4. doi: 10.1002/ajmg.1320340403. Am J Med Genet. 1989. PMID: 2624254
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