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1,414 results
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Slow acetylator mutations in the human polymorphic N-acetyltransferase gene in 786 Asians, blacks, Hispanics, and whites: application to metabolic epidemiology.
Lin HJ, Han CY, Lin BK, Hardy S. Lin HJ, et al. Among authors: lin bk. Am J Hum Genet. 1993 Apr;52(4):827-34. Am J Hum Genet. 1993. PMID: 8460648 Free PMC article.
Methanol for preparing hair bulbs for PCR.
Han CY, Lin BK, Lin HJ. Han CY, et al. Among authors: lin hj, lin bk. Nucleic Acids Res. 1992 Dec 11;20(23):6419-20. doi: 10.1093/nar/20.23.6419. Nucleic Acids Res. 1992. PMID: 1475208 Free PMC article.
Functional profile of the human fetal gamma-globin gene upstream promoter region.
Lin HJ, Han CY, Nienhuis AW. Lin HJ, et al. Am J Hum Genet. 1992 Aug;51(2):363-70. Am J Hum Genet. 1992. PMID: 1642236 Free PMC article.
Molecular basis of beta thalassemia in south China. Strategy for DNA analysis.
Zhang JZ, Cai SP, He X, Lin HX, Lin HJ, Huang ZG, Chehab FF, Kan YW. Zhang JZ, et al. Among authors: lin hj, lin hx. Hum Genet. 1988 Jan;78(1):37-40. doi: 10.1007/BF00291231. Hum Genet. 1988. PMID: 3338793
Ethnic distribution of the glutathione transferase Mu 1-1 (GSTM1) null genotype in 1473 individuals and application to bladder cancer susceptibility.
Lin HJ, Han CY, Bernstein DA, Hsiao W, Lin BK, Hardy S. Lin HJ, et al. Among authors: lin bk. Carcinogenesis. 1994 May;15(5):1077-81. doi: 10.1093/carcin/15.5.1077. Carcinogenesis. 1994. PMID: 8200072
DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): a new patient and delineation of neurologic variability among recessive cases.
Lin HJ, Kakkis ED, Eteson DJ, Lachman RS. Lin HJ, et al. Am J Med Genet. 1993 Sep 15;47(4):534-9. doi: 10.1002/ajmg.1320470419. Am J Med Genet. 1993. PMID: 8256819
Exstrophy of the cloaca in a 47,XXX child: review of genitourinary malformations in triple-X patients.
Lin HJ, Ndiforchu F, Patell S. Lin HJ, et al. Am J Med Genet. 1993 Mar 15;45(6):761-3. doi: 10.1002/ajmg.1320450619. Am J Med Genet. 1993. PMID: 8456857 Review.
Microdontia with severe microcephaly and short stature in two brothers: osteodysplastic primordial dwarfism with dental findings.
Lin HJ, Sue GY, Berkowitz CD, Brasel JA, Lachman RS. Lin HJ, et al. Am J Med Genet. 1995 Aug 28;58(2):136-42. doi: 10.1002/ajmg.1320580209. Am J Med Genet. 1995. PMID: 8533804 Review.
Occipital encephalocele and MURCS association: case report and review of central nervous system anomalies in MURCS patients.
Lin HJ, Cornford ME, Hu B, Rutgers JK, Beall MH, Lachman RS. Lin HJ, et al. Am J Med Genet. 1996 Jan 2;61(1):59-62. doi: 10.1002/(SICI)1096-8628(19960102)61:1<59::AID-AJMG11>3.0.CO;2-V. Am J Med Genet. 1996. PMID: 8741919 Review.
Novel p53 mutation in a malignant tumor secreting vasoactive intestinal peptide.
Lin HJ, French SW, Reichenbach D, Wan YJ, Passaro E Jr, Sawicki MP. Lin HJ, et al. Arch Pathol Lab Med. 1997 Feb;121(2):125-8. Arch Pathol Lab Med. 1997. PMID: 9126038
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