Smith KD - Search Results

1

A molecular basis for hemoglobin-H disease in American blacks.

Phillips JA 3rd, Scott AF, Smith KD, Young KE, Lightbody KL, Jiji RM, Kazazian HH Jr. Phillips JA 3rd, et al. Among authors: smith kd. Blood. 1979 Dec;54(6):1439-45. Blood. 1979. PMID: 508947 Free article.

2

Unequal crossing-over: a common basis of single alpha-globin genes in Asians and American blacks with hemoglobin-H disease.

Phillips JA 3rd, Vik TA, Scott AF, Young KE, Kazazian HH Jr, Smith KD, Fairbanks VF, Koenig HM. Phillips JA 3rd, et al. Among authors: smith kd. Blood. 1980 Jun;55(6):1066-9. Blood. 1980. PMID: 6246995 Free article.

3

The molecular basis of hemoglobin Grady.

Scott AF, Phillips JA 3rd, Young KE, Kazazian HH Jr, Smith KD, Charache S, Clegg JB. Scott AF, et al. Among authors: smith kd. Am J Hum Genet. 1981 Jan;33(1):129-33. Am J Hum Genet. 1981. PMID: 6258429 Free PMC article.

4

Prenatal diagnosis of sickle cell anemia by restriction and endonuclease analysis: HindIII polymorphisms in gamma-globin genes extend test applicability.

Phillips JA 3rd, Panny SR, Kazazian HH Jr, Boehm CD, Scott AF, Smith KD. Phillips JA 3rd, et al. Among authors: smith kd. Proc Natl Acad Sci U S A. 1980 May;77(5):2853-6. doi: 10.1073/pnas.77.5.2853. Proc Natl Acad Sci U S A. 1980. PMID: 6248872 Free PMC article.

5

Prenatal diagnosis of hemoglobinopathies by restriction endonuclease analysis: pregnancies at risk for sickle cell anemia and S--O Arab disease.

Phillips JA 3rd, Scott AF, Kazazian HH Jr, Smith KD, Stetten G, Thomas GH. Phillips JA 3rd, et al. Among authors: smith kd. Johns Hopkins Med J. 1979 Aug;145(2):57-60. Johns Hopkins Med J. 1979. PMID: 459205 No abstract available.

6

Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosis.

Panny SR, Scott AF, Smith KD, Phillips JA 3rd, Kazazian HH Jr, Talbot CC Jr, Boehm CD. Panny SR, et al. Among authors: smith kd. Am J Hum Genet. 1981 Jan;33(1):25-35. Am J Hum Genet. 1981. PMID: 6162380 Free PMC article.

7

Transcripts homologous to a long repeated DNA element in the human genome.

Schmeckpeper BJ, Scott AF, Smith KD. Schmeckpeper BJ, et al. Among authors: smith kd. J Biol Chem. 1984 Jan 25;259(2):1218-25. J Biol Chem. 1984. PMID: 6198321 Free article.

8

Repeated DNA of the human Y chromosome.

Smith KD, Young KE, Talbot CC Jr, Schmeckpeper BJ. Smith KD, et al. Development. 1987;101 Suppl:77-92. doi: 10.1242/dev.101.Supplement.77. Development. 1987. PMID: 2846258

9

Use of repetitive DNA for diagnosis of chromosomal rearrangements.

Burk RD, Stamberg J, Young KE, Smith KD. Burk RD, et al. Among authors: smith kd. Hum Genet. 1983;64(4):339-42. doi: 10.1007/BF00292365. Hum Genet. 1983. PMID: 6311727

10

The proportion of all point mutations which are unacceptable: an estimate based on hemoglobin amino acid and nucleotide sequences.

Boyer SH, Scott AF, Kunkel LM, Smith KD. Boyer SH, et al. Among authors: smith kd. Can J Genet Cytol. 1978 Mar;20(1):111-37. doi: 10.1139/g78-013. Can J Genet Cytol. 1978. PMID: 350360

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