Similar articles for PMID: 12707965

Year	Number of Results
1980	1
1995	5
1996	9
1997	5
1998	10
1999	8
2000	12
2001	5
2002	6
2003	8
2004	1
2005	2
2012	4
2013	4
2014	4
2015	2
2016	4
2017	5
2018	5
2019	1
2020	1
2021	3
2022	2
2024	0

1

Hypochondroplasia and stature within normal limits: another family with an Asn540Ser mutation in the fibroblast growth factor receptor 3 gene.

Thauvin-Robinet C, Faivre L, Lewin P, De Monléon JV, François C, Huet F, Couailler JF, Campos-Xavier AB, Bonaventure J, Le Merrer M. Thauvin-Robinet C, et al. Am J Med Genet A. 2003 May 15;119A(1):81-4. doi: 10.1002/ajmg.a.10238. Am J Med Genet A. 2003. PMID: 12707965 No abstract available.

2

Clinical and radiologic evaluation of a Turkish family with hypochondroplasia and a rare FGFR3 variant.

Ekinci S, Ülger Y, Acar MO, Ceran A, Aycan Z, Fitoz ÖS, Ilgın Ruhi H. Ekinci S, et al. J Pediatr Endocrinol Metab. 2022 Apr 20;35(8):1097-1101. doi: 10.1515/jpem-2021-0773. Print 2022 Aug 26. J Pediatr Endocrinol Metab. 2022. PMID: 35438268

3

Hypochondroplasia and temporal lobe epilepsy - A series of 4 cases.

Ahmadi M, Herting A, Mueffelmann B, Woermann FG, Abou Jamra R, Bien CG, Polster T, Brandt C. Ahmadi M, et al. Epilepsy Behav. 2022 Jan;126:108479. doi: 10.1016/j.yebeh.2021.108479. Epub 2021 Dec 16. Epilepsy Behav. 2022. PMID: 34922328

4

New Magnetic Resonance Imaging (MRI) findings in a patient with hypochondroplasia caused by the FGFR3 N540K variant.

Mimura PMP, Castro JTS, Jarry VM, França Júnior MC, Reis F. Mimura PMP, et al. Arq Neuropsiquiatr. 2021 Jul;79(7):656-657. doi: 10.1590/0004-282X-ANP-2020-0424. Arq Neuropsiquiatr. 2021. PMID: 34133497 Free article. No abstract available.

5

Genome reveals giraffe's recipe for standing tall.

Moutinho S. Moutinho S. Science. 2021 Mar 19;371(6535):1190. doi: 10.1126/science.371.6535.1190. Science. 2021. PMID: 33737467 No abstract available.

6

A case of dwarfism in 6th century Italy: Bioarchaeological assessment of a hereditary disorder.

Traversari M, Da Via S, Petrella E, Feeney RNM, Benazzi S. Traversari M, et al. Int J Paleopathol. 2020 Sep;30:110-117. doi: 10.1016/j.ijpp.2020.03.003. Epub 2020 Jun 30. Int J Paleopathol. 2020. PMID: 32619963

7

Acanthosis nigricans, hypochondroplasia, and FGFR3 mutations: Findings with five new patients, and a review of the literature.

Muguet Guenot L, Aubert H, Isidor B, Toutain A, Mazereeuw-Hautier J, Collet C, Bourrat E, Denis Musquer M, Barbarot S; Groupe de Recherche de la Société Française de Dermatologie Pédiatrique. Muguet Guenot L, et al. Pediatr Dermatol. 2019 Mar;36(2):242-246. doi: 10.1111/pde.13748. Epub 2019 Feb 14. Pediatr Dermatol. 2019. PMID: 30762251 Review.

8

FGFR3-related hypochondroplasia: longitudinal growth in 57 children with the p.Asn540Lys mutation.

Arenas MA, Del Pino M, Fano V. Arenas MA, et al. J Pediatr Endocrinol Metab. 2018 Nov 27;31(11):1279-1284. doi: 10.1515/jpem-2018-0046. J Pediatr Endocrinol Metab. 2018. PMID: 30335613

9

Familial acanthosis nigricans with the FGFR3 mutation: Differences of pigmentation between male and female patients.

Yasuda M, Morimoto N, Shimizu A, Toyoshima T, Yokoyama Y, Ishikawa O. Yasuda M, et al. J Dermatol. 2018 Nov;45(11):1357-1361. doi: 10.1111/1346-8138.14623. Epub 2018 Aug 31. J Dermatol. 2018. PMID: 30168875

10

Further delineation of achondroplasia-hypochondroplasia complex with long-term survival.

González-Del Angel A, Rius R, Alcántara-Ortigoza MA, Spector E, Del Castillo V, Mata-García LE. González-Del Angel A, et al. Am J Med Genet A. 2018 May;176(5):1225-1231. doi: 10.1002/ajmg.a.38660. Am J Med Genet A. 2018. PMID: 29681095 Review.

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