Similar articles for PMID: 10395236

Year	Number of Results
1994	2
1995	5
1996	11
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1998	12
1999	10
2000	8
2001	8
2002	5
2003	8
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2005	5
2006	4
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2013	2
2014	2
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2018	1
2019	2
2020	1
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2022	1
2023	1
2024	0

1

A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasia.

Fofanova OV, Takamura N, Kinoshita E, Meerson EM, Iljina VK, Nechvolodova OL, Evgrafov OV, Peterkova VA, Yamashita S. Fofanova OV, et al. Endocr J. 1998 Dec;45(6):791-5. doi: 10.1507/endocrj.45.791. Endocr J. 1998. PMID: 10395236 Free article.

2

[Mutations in the Fibroblast Growth Factor Receptor 3 gene (FGFR3) in Chilean patients with idiopathic short stature, hypochondroplasia and achondroplasia].

Mancilla EE, Poggi H, Repetto G, García C, Foradori A, Cattani A. Mancilla EE, et al. Rev Med Chil. 2003 Dec;131(12):1405-10. Rev Med Chil. 2003. PMID: 15022403 Spanish.

3

A common FGFR3 gene mutation in hypochondroplasia.

Prinos P, Costa T, Sommer A, Kilpatrick MW, Tsipouras P. Prinos P, et al. Hum Mol Genet. 1995 Nov;4(11):2097-101. doi: 10.1093/hmg/4.11.2097. Hum Mol Genet. 1995. PMID: 8589686

4

A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia.

Bellus GA, McIntosh I, Smith EA, Aylsworth AS, Kaitila I, Horton WA, Greenhaw GA, Hecht JT, Francomano CA. Bellus GA, et al. Nat Genet. 1995 Jul;10(3):357-9. doi: 10.1038/ng0795-357. Nat Genet. 1995. PMID: 7670477

5

Genotype phenotype correlation in achondroplasia and hypochondroplasia.

Matsui Y, Yasui N, Kimura T, Tsumaki N, Kawabata H, Ochi T. Matsui Y, et al. J Bone Joint Surg Br. 1998 Nov;80(6):1052-6. doi: 10.1302/0301-620x.80b6.9277. J Bone Joint Surg Br. 1998. PMID: 9853502

6

Common mutations in the fibroblast growth factor receptor 3 (FGFR 3) gene account for achondroplasia, hypochondroplasia, and thanatophoric dwarfism.

Bonaventure J, Rousseau F, Legeai-Mallet L, Le Merrer M, Munnich A, Maroteaux P. Bonaventure J, et al. Am J Med Genet. 1996 May 3;63(1):148-54. doi: 10.1002/(SICI)1096-8628(19960503)63:1<148::AID-AJMG26>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8723101

7

Clinical and genetic heterogeneity of hypochondroplasia.

Rousseau F, Bonaventure J, Legeai-Mallet L, Schmidt H, Weissenbach J, Maroteaux P, Munnich A, Le Merrer M. Rousseau F, et al. J Med Genet. 1996 Sep;33(9):749-52. doi: 10.1136/jmg.33.9.749. J Med Genet. 1996. PMID: 8880574 Free PMC article.

8

A novel missense mutation Ile538Val in the fibroblast growth factor receptor 3 in hypochondroplasia. Mutations in brief no. 122. Online.

Grigelioniené G, Hagenäs L, Eklöf O, Neumeyer L, Haereid PE, Anvret M. Grigelioniené G, et al. Hum Mutat. 1998;11(4):333. doi: 10.1002/(SICI)1098-1004(1998)11:4<333::AID-HUMU18>3.0.CO;2-G. Hum Mutat. 1998. PMID: 10215410

9

Molecularly proven hypochondroplasia with cloverleaf skull deformity: a novel association.

Angle B, Hersh JH, Christensen KM. Angle B, et al. Clin Genet. 1998 Nov;54(5):417-20. doi: 10.1111/j.1399-0004.1998.tb03756.x. Clin Genet. 1998. PMID: 9842995

10

Asn540Lys mutation in fibroblast growth factor receptor 3 and phenotype in hypochondroplasia.

Grigelioniené G, Eklöf O, Laurencikas E, Ollars B, Hertel NT, Dumanski JP, Hagenäs L. Grigelioniené G, et al. Acta Paediatr. 2000 Sep;89(9):1072-6. doi: 10.1080/713794579. Acta Paediatr. 2000. PMID: 11071087

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