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A locus for autosomal recessive achromatopsia on human chromosome 8q.
Milunsky A, Huang XL, Milunsky J, DeStefano A, Baldwin CT. Milunsky A, et al. Among authors: baldwin ct. Clin Genet. 1999 Jul;56(1):82-5. doi: 10.1034/j.1399-0004.1999.560112.x. Clin Genet. 1999. PMID: 10466422
Linkage of chromosome 13q32 to schizophrenia in a large veterans affairs cooperative study sample.
Faraone SV, Skol AD, Tsuang DW, Bingham S, Young KA, Prabhudesai S, Haverstock SL, Mena F, Menon AS, Bisset D, Pepple J, Sautter F, Baldwin C, Weiss D, Collins J, Keith T, Boehnke M, Tsuang MT, Schellenberg GD. Faraone SV, et al. Among authors: baldwin c. Am J Med Genet. 2002 Aug 8;114(6):598-604. doi: 10.1002/ajmg.10601. Am J Med Genet. 2002. PMID: 12210272
Polymorphisms near a chromosome 6q QTL area are associated with modulation of fetal hemoglobin levels in sickle cell anemia.
Wyszynski DF, Baldwin CT, Cleves MA, Amirault Y, Nolan VG, Farrell JJ, Bisbee A, Kutlar A, Farrer LA, Steinberg MH. Wyszynski DF, et al. Among authors: baldwin ct. Cell Mol Biol (Noisy-le-grand). 2004 Feb;50(1):23-33. Cell Mol Biol (Noisy-le-grand). 2004. PMID: 15040424
Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea.
Ma Q, Wyszynski DF, Farrell JJ, Kutlar A, Farrer LA, Baldwin CT, Steinberg MH. Ma Q, et al. Among authors: baldwin ct. Pharmacogenomics J. 2007 Dec;7(6):386-94. doi: 10.1038/sj.tpj.6500433. Epub 2007 Feb 13. Pharmacogenomics J. 2007. PMID: 17299377 Clinical Trial.
Evidence for genetic heterogeneity of the Carney complex (familial atrial myxoma syndromes).
Milunsky J, Huang XL, Baldwin CT, Farah MG, Milunsky A. Milunsky J, et al. Among authors: baldwin ct. Cancer Genet Cytogenet. 1998 Oct 15;106(2):173-6. doi: 10.1016/s0165-4608(98)00063-6. Cancer Genet Cytogenet. 1998. PMID: 9797786
Autosomal dominant orthostatic hypotensive disorder maps to chromosome 18q.
DeStefano AL, Baldwin CT, Burzstyn M, Gavras I, Handy DE, Joost O, Martel T, Nicolaou M, Schwartz F, Streeten DH, Farrer LA, Gavras H. DeStefano AL, et al. Among authors: baldwin ct. Am J Hum Genet. 1998 Nov;63(5):1425-30. doi: 10.1086/302096. Am J Hum Genet. 1998. PMID: 9792870 Free PMC article.
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations.
DeStefano AL, Cupples LA, Arnos KS, Asher JH Jr, Baldwin CT, Blanton S, Carey ML, da Silva EO, Friedman TB, Greenberg J, Lalwani AK, Milunsky A, Nance WE, Pandya A, Ramesar RS, Read AP, Tassabejhi M, Wilcox ER, Farrer LA. DeStefano AL, et al. Among authors: baldwin ct. Hum Genet. 1998 May;102(5):499-506. doi: 10.1007/s004390050732. Hum Genet. 1998. PMID: 9654197
Familial paragangliomas: linkage to chromosome 11q23 and clinical implications.
Milunsky J, DeStefano AL, Huang XL, Baldwin CT, Michels VV, Jako G, Milunsky A. Milunsky J, et al. Among authors: baldwin ct. Am J Med Genet. 1997 Oct 3;72(1):66-70. doi: 10.1002/(sici)1096-8628(19971003)72:1<66::aid-ajmg14>;2-s. Am J Med Genet. 1997. PMID: 9295078
Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population.
Baldwin CT, Weiss S, Farrer LA, De Stefano AL, Adair R, Franklyn B, Kidd KK, Korostishevsky M, Bonné-Tamir B. Baldwin CT, et al. Hum Mol Genet. 1995 Sep;4(9):1637-42. doi: 10.1093/hmg/4.9.1637. Hum Mol Genet. 1995. PMID: 8541853
Mutations in PAX3 that cause Waardenburg syndrome type I: ten new mutations and review of the literature.
Baldwin CT, Hoth CF, Macina RA, Milunsky A. Baldwin CT, et al. Am J Med Genet. 1995 Aug 28;58(2):115-22. doi: 10.1002/ajmg.1320580205. Am J Med Genet. 1995. PMID: 8533800 Review.
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