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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1997 | 1 |
1998 | 3 |
1999 | 1 |
2000 | 1 |
2024 | 0 |
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6 results
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Page 1
Acromesomelic dysplasia Maroteaux type maps to human chromosome 9.
Am J Hum Genet. 1998 Jul;63(1):155-62. doi: 10.1086/301917.
Am J Hum Genet. 1998.
PMID: 9634515
Free PMC article.
Autosomal recessive disorder otospondylomegaepiphyseal dysplasia is associated with loss-of-function mutations in the COL11A2 gene.
Melkoniemi M, Brunner HG, Manouvrier S, Hennekam R, Superti-Furga A, Kääriäinen H, Pauli RM, van Essen T, Warman ML, Bonaventure J, Miny P, Ala-Kokko L.
Melkoniemi M, et al.
Am J Hum Genet. 2000 Feb;66(2):368-77. doi: 10.1086/302750.
Am J Hum Genet. 2000.
PMID: 10677296
Free PMC article.
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The camptodactyly-arthropathy-coxa vara-pericarditis syndrome: clinical features and genetic mapping to human chromosome 1.
Bahabri SA, Suwairi WM, Laxer RM, Polinkovsky A, Dalaan AA, Warman ML.
Bahabri SA, et al.
Arthritis Rheum. 1998 Apr;41(4):730-5. doi: 10.1002/1529-0131(199804)41:4<730::AID-ART22>3.0.CO;2-Y.
Arthritis Rheum. 1998.
PMID: 9550484
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Mutations in CDMP1 cause autosomal dominant brachydactyly type C.
Polinkovsky A, Robin NH, Thomas JT, Irons M, Lynn A, Goodman FR, Reardon W, Kant SG, Brunner HG, van der Burgt I, Chitayat D, McGaughran J, Donnai D, Luyten FP, Warman ML.
Polinkovsky A, et al.
Nat Genet. 1997 Sep;17(1):18-9. doi: 10.1038/ng0997-18.
Nat Genet. 1997.
PMID: 9288091
Free article.
No abstract available.
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Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis.
Gong Y, Krakow D, Marcelino J, Wilkin D, Chitayat D, Babul-Hirji R, Hudgins L, Cremers CW, Cremers FP, Brunner HG, Reinker K, Rimoin DL, Cohn DH, Goodman FR, Reardon W, Patton M, Francomano CA, Warman ML.
Gong Y, et al.
Nat Genet. 1999 Mar;21(3):302-4. doi: 10.1038/6821.
Nat Genet. 1999.
PMID: 10080184
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Stickler syndrome without eye involvement is caused by mutations in COL11A2, the gene encoding the alpha2(XI) chain of type XI collagen.
Sirko-Osadsa DA, Murray MA, Scott JA, Lavery MA, Warman ML, Robin NH.
Sirko-Osadsa DA, et al.
J Pediatr. 1998 Feb;132(2):368-71. doi: 10.1016/s0022-3476(98)70466-4.
J Pediatr. 1998.
PMID: 9506662
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