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Year | Number of Results |
---|---|
1978 | 1 |
1980 | 1 |
1982 | 1 |
1998 | 1 |
1999 | 1 |
2024 | 0 |
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Page 1
Identification of GTF2IRD1, a putative transcription factor within the Williams-Beuren syndrome deletion at 7q11.23.
Cytogenet Cell Genet. 1999;86(3-4):296-304. doi: 10.1159/000015322.
Cytogenet Cell Genet. 1999.
PMID: 10575229
Managers, educators collaborate for hospitalwide educational programs.
Lawrence D, Peoples RJ.
Lawrence D, et al. Among authors: peoples rj.
Hosp Prog. 1982 Sep;63(9):36-9, 60.
Hosp Prog. 1982.
PMID: 10256561
No abstract available.
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Identification of the WBSCR9 gene, encoding a novel transcriptional regulator, in the Williams-Beuren syndrome deletion at 7q11.23.
Peoples RJ, Cisco MJ, Kaplan P, Francke U.
Peoples RJ, et al.
Cytogenet Cell Genet. 1998;82(3-4):238-46. doi: 10.1159/000015110.
Cytogenet Cell Genet. 1998.
PMID: 9858827
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Patient representatives assure hospital accountability.
Peoples RJ.
Peoples RJ.
Mich Hosp. 1980 Dec;16(12):8-10.
Mich Hosp. 1980.
PMID: 10249137
No abstract available.
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The hospital as intermediary: from the eyes of Daniel Webster.
Peoples RJ.
Peoples RJ.
Mich Hosp. 1978 May;14(5):27.
Mich Hosp. 1978.
PMID: 10308435
No abstract available.
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