Overton KM - Search Results

1

Parental origin of a ring 13 chromosome in a female with multiple anomalies.

Magenis RE, Wyandt HE, Overton KM, Macfarlane J. Magenis RE, et al. Among authors: overton km. Hum Genet. 1976 Jul 27;33(2):181-6. doi: 10.1007/BF00281894. Hum Genet. 1976. PMID: 939570

2

Parental origin of the extra chromosome in Down's syndrome.

Magenis RE, Overton KM, Chamberlin J, Brady T, Lovrien E. Magenis RE, et al. Among authors: overton km. Hum Genet. 1977 Jun 10;37(1):7-16. doi: 10.1007/BF00293766. Hum Genet. 1977. PMID: 142063

3

Linkage relationships of HLA and a familial chromosome 6 inversion (pter leads to p23::q23 leads to qter): lack of dose effect in duplication-deficient offspring.

Magenis RE, Chamberlin J, Overton K, Lovrien E. Magenis RE, et al. Cytogenet Cell Genet. 1978;22(1-6):418-20. doi: 10.1159/000130987. Cytogenet Cell Genet. 1978. PMID: 752516 No abstract available.

4

Cytogenetic darkroom magic: now you see them, now you don't.

Overton KM, Magenis RE, Brady T, Chamberlin J, Parks M. Overton KM, et al. Am J Hum Genet. 1976 Jul;28(4):417-9. Am J Hum Genet. 1976. PMID: 133609 Free PMC article.

5

Further evidence for the assignment of the red cell acid phosphatase gene (ACP1) to the short arm of chromosome 2 from gene dosage effect.

Magenis RE, Koler RD, Lovrien E, Bigley RH, DuVal MC, Overton KM. Magenis RE, et al. Among authors: overton km. Cytogenet Cell Genet. 1976;16(1-5):326-7. doi: 10.1159/000130622. Cytogenet Cell Genet. 1976. PMID: 975901 No abstract available.

6

Exclusion gene mapping utilizing patients with chromosome imbalance: the HL-A system as a prototype.

Magenis RE, Overton K, Wyandt H, Bergstrom T, Hecht F, Lovrien E. Magenis RE, et al. Humangenetik. 1975;27(2):91-109. doi: 10.1007/BF00273324. Humangenetik. 1975. PMID: 1150239

7

Gene dosage: evidence for assignment of erythrocyte acid phosphatase locus to chromosome 2.

Magenis RE, Koler RD, Lovrien E, Bigley RH, DuVal MC, Overton KM. Magenis RE, et al. Among authors: overton km. Proc Natl Acad Sci U S A. 1975 Nov;72(11):4526-30. doi: 10.1073/pnas.72.11.4526. Proc Natl Acad Sci U S A. 1975. PMID: 1060135 Free PMC article.

8

Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome II.

Magenis RE, Armendares S, Hecht F, Weleber RG, Overton K. Magenis RE, et al. Ann Genet. 1972 Dec;15(4):265. Ann Genet. 1972. PMID: 4539485 No abstract available.

9

Partial trisomy 15.

Magenis RE, Overton KM, Reiss JA, Macfarlane JP, Hecht F. Magenis RE, et al. Among authors: overton km. Lancet. 1972 Dec 23;2(7791):1365-6. doi: 10.1016/s0140-6736(72)92806-1. Lancet. 1972. PMID: 4118227 No abstract available.

10

Further evidence for the assignment of the red cell acid phosphatase gene (ACP1) to the short arm of chromosome 2 from gene dosage effect.

Magenis RE, Koler RD, Lovrien E, Bigley RH, DuVal MC, Overton KM. Magenis RE, et al. Among authors: overton km. Birth Defects Orig Artic Ser. 1976;12(7):326-7. Birth Defects Orig Artic Ser. 1976. PMID: 1024633 No abstract available.

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