Dobbs M - Search Results

1

Molecular analysis of a case of meiotic recombination leading to cri-du-chat syndrome.

Dobbs M, Overhauser J, Wasmuth JJ. Dobbs M, et al. Cytogenet Cell Genet. 1988;47(1-2):5-7. doi: 10.1159/000132493. Cytogenet Cell Genet. 1988. PMID: 3356169

2

Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5.

Nakamura Y, Lathrop M, Leppert M, Dobbs M, Wasmuth J, Wolff E, Carlson M, Fujimoto E, Krapcho K, Sears T, et al. Nakamura Y, et al. Among authors: dobbs m. Am J Hum Genet. 1988 Nov;43(5):638-44. Am J Hum Genet. 1988. PMID: 2903664 Free PMC article.

3

An anonymous DNA segment pTP5E (D5S70) maps to the long arm of chromosome 5 and identifies a Taq I polymorphism.

Farber RA, Phalen T, Neuman WL, Le Beau MM, Wasmuth JJ, Dobbs M. Farber RA, et al. Among authors: dobbs m. Nucleic Acids Res. 1988 Mar 25;16(5):2360. doi: 10.1093/nar/16.5.2360. Nucleic Acids Res. 1988. PMID: 2895914 Free PMC article.

4

Localization of a susceptibility locus for schizophrenia on chromosome 5.

Sherrington R, Brynjolfsson J, Petursson H, Potter M, Dudleston K, Barraclough B, Wasmuth J, Dobbs M, Gurling H. Sherrington R, et al. Among authors: dobbs m. Nature. 1988 Nov 10;336(6195):164-7. doi: 10.1038/336164a0. Nature. 1988. PMID: 2903449

5

The gene for familial polyposis coli maps to the long arm of chromosome 5.

Leppert M, Dobbs M, Scambler P, O'Connell P, Nakamura Y, Stauffer D, Woodward S, Burt R, Hughes J, Gardner E, et al. Leppert M, et al. Among authors: dobbs m. Science. 1987 Dec 4;238(4832):1411-3. doi: 10.1126/science.3479843. Science. 1987. PMID: 3479843

6

Asymmetric lower-limb malformations in individuals with homeobox PITX1 gene mutation.

Gurnett CA, Alaee F, Kruse LM, Desruisseau DM, Hecht JT, Wise CA, Bowcock AM, Dobbs MB. Gurnett CA, et al. Among authors: dobbs mb. Am J Hum Genet. 2008 Nov;83(5):616-22. doi: 10.1016/j.ajhg.2008.10.004. Epub 2008 Oct 23. Am J Hum Genet. 2008. PMID: 18950742 Free PMC article.

7

Familial isolated clubfoot is associated with recurrent chromosome 17q23.1q23.2 microduplications containing TBX4.

Alvarado DM, Aferol H, McCall K, Huang JB, Techy M, Buchan J, Cady J, Gonzales PR, Dobbs MB, Gurnett CA. Alvarado DM, et al. Among authors: dobbs mb. Am J Hum Genet. 2010 Jul 9;87(1):154-60. doi: 10.1016/j.ajhg.2010.06.010. Am J Hum Genet. 2010. PMID: 20598276 Free PMC article.

8

Rare and de novo coding variants in chromodomain genes in Chiari I malformation.

Sadler B, Wilborn J, Antunes L, Kuensting T, Hale AT, Gannon SR, McCall K, Cruchaga C, Harms M, Voisin N, Reymond A, Cappuccio G, Brunetti-Pierri N, Tartaglia M, Niceta M, Leoni C, Zampino G, Ashley-Koch A, Urbizu A, Garrett ME, Soldano K, Macaya A, Conrad D, Strahle J, Dobbs MB, Turner TN, Shannon CN, Brockmeyer D, Limbrick DD, Gurnett CA, Haller G. Sadler B, et al. Among authors: dobbs mb. Am J Hum Genet. 2021 Jan 7;108(1):100-114. doi: 10.1016/j.ajhg.2020.12.001. Epub 2020 Dec 21. Am J Hum Genet. 2021. PMID: 33352116 Free PMC article.

9

Localization of dominantly inherited isolated triphalangeal thumb to chromosomal region 7q36.

Dobbs MB, Dietz FR, Gurnett CA, Morcuende JA, Steyers CM, Murray JC. Dobbs MB, et al. J Orthop Res. 2000 May;18(3):340-4. doi: 10.1002/jor.1100180303. J Orthop Res. 2000. PMID: 10937618

10

Evidence for an additional locus for split hand/foot malformation in chromosome region 8q21.11-q22.3.

Gurnett CA, Dobbs MB, Nordsieck EJ, Keppel C, Goldfarb CA, Morcuende JA, Bowcock AM. Gurnett CA, et al. Among authors: dobbs mb. Am J Med Genet A. 2006 Aug 15;140(16):1744-8. doi: 10.1002/ajmg.a.31375. Am J Med Genet A. 2006. PMID: 16838310

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