Acrocephalosyndactylia research, articles, guidelines & medical evidence database search.
Access the latest scientific research and medical evidence related to Acrocephalosyndactylia treatment, diagnosis and symptoms, quickly and easily with doctorAsyou.
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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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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
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Unblending of Transcriptional Condensates in Human Repeat Expansion Disease.
Basu Shaon, Mackowiak Sebastian D, Niskanen Henri, Knezevic Dora, Asimi Vahid ...
Cell Vol 181(5)
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Date 28 May 2020
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
hobo is responsible for the induction of hybrid dysgenesis by strains of Drosophila melanogaster bearing the male recombination factor 23.5MRF.
Yannopoulos G, Stamatis N, Monastirioti M, Hatzopoulos P, Louis C
Cell Vol 49(4)
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Date 22 May 1987
Research
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis.
Jabs E W, Müller U, Li X, Ma L, Luo W ...
Cell Vol 75(3)
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Date 05 Nov 1993
Research
A mechanism for gene-environment interaction in the etiology of congenital scoliosis.
Sparrow Duncan B, Chapman Gavin, Smith Allanceson J, Mattar Muhammad Z, Major Joelene A ...
Cell Vol 149(2)
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Date 13 Apr 2012
Research
WT-1 is required for early kidney development.
Kreidberg J A, Sariola H, Loring J M, Maeda M, Pelletier J ...
Cell Vol 74(4)
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Date 27 Aug 1993
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