Buetow K - Search Results

1

Identification and genetic mapping of a homeobox gene to the 4p16.1 region of human chromosome 4.

Stadler HS, Padanilam BJ, Buetow K, Murray JC, Solursh M. Stadler HS, et al. Among authors: buetow k. Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11579-83. doi: 10.1073/pnas.89.23.11579. Proc Natl Acad Sci U S A. 1992. PMID: 1360670 Free PMC article.

2

Characterization of the human HOX 7 cDNA and identification of polymorphic markers.

Padanilam BJ, Stadler HS, Mills KA, McLeod LB, Solursh M, Lee B, Ramirez F, Buetow KH, Murray JC. Padanilam BJ, et al. Among authors: buetow kh. Hum Mol Genet. 1992 Sep;1(6):407-10. doi: 10.1093/hmg/1.6.407. Hum Mol Genet. 1992. PMID: 1284527

3

Genetic and physical maps of human chromosome 4 based on dinucleotide repeats.

Mills KA, Buetow KH, Xu Y, Weber JL, Altherr MR, Wasmuth JJ, Murray JC. Mills KA, et al. Among authors: buetow kh. Genomics. 1992 Oct;14(2):209-19. doi: 10.1016/s0888-7543(05)80208-3. Genomics. 1992. PMID: 1427835

4

Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD).

Mills KA, Buetow KH, Xu Y, Ritty TM, Mathews KD, Bodrug SE, Wijmenga C, Balazs I, Murray JC. Mills KA, et al. Among authors: buetow kh. Am J Hum Genet. 1992 Aug;51(2):432-9. Am J Hum Genet. 1992. PMID: 1642243 Free PMC article.

5

Mapping of the human complement factor I gene to 4q25.

Shiang R, Murray JC, Morton CC, Buetow KH, Wasmuth JJ, Olney AH, Sanger WG, Goldberger G. Shiang R, et al. Among authors: buetow kh. Genomics. 1989 Jan;4(1):82-6. doi: 10.1016/0888-7543(89)90318-2. Genomics. 1989. PMID: 2563353

6

Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4.

Murray JC, Bennett SR, Kwitek AE, Small KW, Schinzel A, Alward WL, Weber JL, Bell GI, Buetow KH. Murray JC, et al. Among authors: buetow kh. Nat Genet. 1992 Sep;2(1):46-9. doi: 10.1038/ng0992-46. Nat Genet. 1992. PMID: 1303248

7

Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35.

Mathews KD, Mills KA, Bosch EP, Ionasescu VV, Wiles KR, Buetow KH, Murray JC. Mathews KD, et al. Among authors: buetow kh. Am J Hum Genet. 1992 Aug;51(2):428-31. Am J Hum Genet. 1992. PMID: 1642242 Free PMC article.

8

The CEPH consortium linkage map of human chromosome 1.

Dracopoli NC, O'Connell P, Elsner TI, Lalouel JM, White RL, Buetow KH, Nishimura DY, Murray JC, Helms C, Mishra SK, et al. Dracopoli NC, et al. Among authors: buetow kh. Genomics. 1991 Apr;9(4):686-700. doi: 10.1016/0888-7543(91)90362-i. Genomics. 1991. PMID: 2037294

9

Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq.

Murray JC, Nishimura DY, Buetow KH, Ardinger HH, Spence MA, Sparkes RS, Falk RE, Falk PM, Gardner RJ, Harkness EM, et al. Murray JC, et al. Among authors: buetow kh. Am J Hum Genet. 1990 Mar;46(3):486-91. Am J Hum Genet. 1990. PMID: 2309700 Free PMC article.

10

Linkage localization of Börjeson-Forssman-Lehmann syndrome.

Mathews KD, Ardinger HH, Nishimura DY, Buetow KH, Murray JC, Bartley JA. Mathews KD, et al. Among authors: buetow kh. Am J Med Genet. 1989 Dec;34(4):470-4. doi: 10.1002/ajmg.1320340403. Am J Med Genet. 1989. PMID: 2624254

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