Abnormalities, Multiple research, articles, guidelines & medical evidence database search.
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All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 18 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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20631 Abstracts
Research
Sociodemographic patterns in spina bifida birth prevalence trends--North Carolina, 1995-1999.
Meyer Robert E, Siega-Riz Anna-Maria
MMWR. Recommendations and reports : Morbidity and mortality weekly rep... Vol 51(RR-13)
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Date 13 Sep 2002
Research
Infant mortality statistics from the 1997 period linked birth/infant death data set.
MacDorman M F, Atkinson J O
National vital statistics reports : from the Centers for Disease Contr... Vol 47(23)
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Date 30 Jul 1999
Research
Births: final data for 2001.
Martin Joyce A, Hamilton Brady E, Ventura Stephanie J, Menacker Fay, Park Melissa M ...
National vital statistics reports : from the Centers for Disease Contr... Vol 51(2)
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Date 18 Dec 2002
Research
Infant mortality statistics from the 1998 period linked birth/infant death data set.
Mathews T J, Curtin S C, MacDorman M F
National vital statistics reports : from the Centers for Disease Contr... Vol 48(12)
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Date 20 Jul 2000
Research
SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder.
Cantagrel Vincent, Lefeber Dirk J, Ng Bobby G, Guan Ziqiang, Silhavy Jennifer L ...
Cell Vol 142(2)
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Date 23 Jul 2010
Research
A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease.
Bruneau B G, Nemer G, Schmitt J P, Charron F, Robitaille L ...
Cell Vol 106(6)
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Date 21 Sep 2001
Research
Human CLP1 mutations alter tRNA biogenesis, affecting both peripheral and central nervous system function.
Karaca Ender, Weitzer Stefan, Pehlivan Davut, Shiraishi Hiroshi, Gogakos Tasos ...
Cell Vol 157(3)
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Date 24 Apr 2014
Research
Function of retinoic acid receptor gamma in the mouse.
Lohnes D, Kastner P, Dierich A, Mark M, LeMeur M ...
Cell Vol 73(4)
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Date 21 May 1993
Research
Mobilization of hobo elements residing within the decapentaplegic gene complex: suggestion of a new hybrid dysgenesis system in Drosophila melanogaste...
Blackman R K, Grimaila R, Koehler M M, Gelbart W M
Cell Vol 49(4)
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Date 22 May 1987
Research
Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome.
Celli J, Duijf P, Hamel B C, Bamshad M, Kramer B ...
Cell Vol 99(2)
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Date 15 Oct 1999
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