Ferrell RE - Search Results

1

Von Recklinghausen neurofibromatosis: a linkage study of candidate and random marker genes.

Ferrell RE, Buetow KH, Darby JK, Eichner JE, Murray JC, Smith R, Waziri M, Huson S, Riccardi VM. Ferrell RE, et al. J Med Genet. 1987 Sep;24(9):522-4. doi: 10.1136/jmg.24.9.522. J Med Genet. 1987. PMID: 3118028 Free PMC article.

2

A genetic linkage study in 15 families of individuals with von Recklinghausen neurofibromatosis.

Dunn BG, Ferrell RE, Riccardi VM. Dunn BG, et al. Among authors: ferrell re. Am J Med Genet. 1985 Oct;22(2):403-7. doi: 10.1002/ajmg.1320220225. Am J Med Genet. 1985. PMID: 3931478

3

A simplified method for screening the apolipoprotein E polymorphism.

Eichner JE, Kuller LH, Ferrell RE, Kamboh MI. Eichner JE, et al. Among authors: ferrell re. Hum Hered. 1991;41(1):61-4. doi: 10.1159/000153976. Hum Hered. 1991. PMID: 2050384

4

Genetic studies of low-abundance human plasma proteins. XII. A new variant of corticosteroid-binding globulin detected by isoelectric focusing/immunoblotting.

Eichner JE, Kamboh MI, Cook T, Ferrell RE. Eichner JE, et al. Among authors: ferrell re. Hum Hered. 1989;39(3):170-3. doi: 10.1159/000153854. Hum Hered. 1989. PMID: 2591981

5

Phenotypic effects of apolipoprotein structural variation on lipid profiles: II. Apolipoprotein A-IV and quantitative lipid measures in the healthy women study.

Eichner JE, Kuller LH, Ferrell RE, Kamboh MI. Eichner JE, et al. Among authors: ferrell re. Genet Epidemiol. 1989;6(4):493-9. doi: 10.1002/gepi.1370060404. Genet Epidemiol. 1989. PMID: 2777070

6

Familial cavernous angiomas: natural history and genetic study over a 5-year period.

Hayman LA, Evans RA, Ferrell RE, Fahr LM, Ostrow P, Riccardi VM. Hayman LA, et al. Among authors: ferrell re. Am J Med Genet. 1982 Feb;11(2):147-60. doi: 10.1002/ajmg.1320110205. Am J Med Genet. 1982. PMID: 6950664

7

An RFLP for glycoprotein A (MN) is in linkage disequilibrium with MN and Ss.

Murray JC, Buetow KH, Ferrell RE, Sieberg PD, Fukuda M. Murray JC, et al. Among authors: ferrell re. Cytogenet Cell Genet. 1988;47(3):149-51. doi: 10.1159/000132534. Cytogenet Cell Genet. 1988. PMID: 2897896

8

A syndrome of microcephaly and retinal pigmentary abnormalities without mental retardation in a family with coincidental autosomal dominant hyperreflexia.

Parke JT, Riccardi VM, Lewis RA, Ferrell RE. Parke JT, et al. Among authors: ferrell re. Am J Med Genet. 1984 Mar;17(3):585-94. doi: 10.1002/ajmg.1320170306. Am J Med Genet. 1984. PMID: 6711609

9

Alpha 2-HS glycoprotein phenotypes and quantitative hormone and bone measures in postmenopausal women.

Eichner JE, Friedrich CA, Cauley JA, Kamboh MI, Gutai JP, Kuller LH, Ferrell RE. Eichner JE, et al. Among authors: ferrell re. Calcif Tissue Int. 1990 Dec;47(6):345-9. doi: 10.1007/BF02555885. Calcif Tissue Int. 1990. PMID: 1705475

10

Phenotypic effects of apolipoprotein structural variation on lipid profiles. IV. Apolipoprotein polymorphisms in a small group of black women from the healthy women study.

Eichner JE, Kuller LH, Ferrell RE, Kamboh MI. Eichner JE, et al. Among authors: ferrell re. Genet Epidemiol. 1989;6(6):681-9. doi: 10.1002/gepi.1370060605. Genet Epidemiol. 1989. PMID: 2606341

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