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Prenatal diagnosis of Freeman-Sheldon syndrome (whistling face).
Prenat Diagn. 1995 Feb;15(2):179-82. doi: 10.1002/pd.1970150212.
Prenat Diagn. 1995.
PMID: 7784371
Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes.
Greenhaw GA, Hebert A, Duke-Woodside ME, Butler IJ, Hecht JT, Cleaver JE, Thomas GH, Horton WA.
Greenhaw GA, et al.
Am J Hum Genet. 1992 Apr;50(4):677-89.
Am J Hum Genet. 1992.
PMID: 1372469
Free PMC article.
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Confirmatory linkage of hypochondroplasia to chromosome arm 4p.
Hecht JT, Herrera CA, Greenhaw GA, Francomano CA, Bellus GA, Blanton SH.
Hecht JT, et al. Among authors: greenhaw ga.
Am J Med Genet. 1995 Jul 3;57(3):505-6. doi: 10.1002/ajmg.1320570333.
Am J Med Genet. 1995.
PMID: 7677163
No abstract available.
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A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia.
Bellus GA, McIntosh I, Smith EA, Aylsworth AS, Kaitila I, Horton WA, Greenhaw GA, Hecht JT, Francomano CA.
Bellus GA, et al. Among authors: greenhaw ga.
Nat Genet. 1995 Jul;10(3):357-9. doi: 10.1038/ng0795-357.
Nat Genet. 1995.
PMID: 7670477
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Concatemers in a rapidly sedimenting, replicating bacteriophage T7 DNA.
Serwer P, Greenhaw GA, Allen JL.
Serwer P, et al. Among authors: greenhaw ga.
Virology. 1982 Dec;123(2):474-9. doi: 10.1016/0042-6822(82)90283-5.
Virology. 1982.
PMID: 6294987
No abstract available.
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