L'hypochondroplasie (à propos de 9 observations personnelles) = HypochondroplasiaFONTAINE, G.Médecine et hygiène. 1984, Vol 42, Num 1552, pp 499-504, issn 0025-6749Article

Hypochondroplasie. Revue de 80 cas = Hypochondroplasia. Review of 80 casesMAROTEAUX, P; FALZON, P.Archives françaises de pédiatrie. 1988, Vol 45, Num 2, pp 105-109, issn 0003-9764Article

Achondroplasia-Hypochondroplasia Complex and Abnormal Pulmonary AnatomyBOBER, Michael B; TAYLOR, Megan; HEINLE, Robert et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 9, pp 2336-2341, issn 1552-4825, 6 p.Article

An autosomal recessive bone dysplasia syndrome resembling hypochondroplasiaDESCH, L. W.Pediatrics (Evanston). 1985, Vol 75, Num 4, pp 786-789, issn 0031-4005Article

Radiological Clues to the Early Diagnosis of Hypochondroplasia in the Neonatal Period: Report of Two PatientsSAITO, Tomoko; NAGASAKI, Keisuke; NISHIMURA, Gen et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 3, pp 630-634, issn 1552-4825, 5 p.Article

Acanthosis Nigricans in a Child With Mild Osteochondrodysplasia and K650Q Mutation in the FGFR3 GeneLEROY, Jules G; NUYTINCK, Lieve; LAMBERT, Jo et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 24, pp 3144-3149, issn 1552-4825, 6 p.Article

Novel FGFR3 mutations creating cysteine residues in the extracellular domain of the receptor cause achondroplasia or severe forms of hypochondroplasiaHEUERTZ, Solange; LE MERRER, Martine; ZABEL, Bernhard et al.European journal of human genetics. 2006, Vol 14, Num 12, pp 1240-1247, issn 1018-4813, 8 p.Article

Prenatal diagnosis of hypochondroplasia : Report of two casesKARADIMAS, C; SIFAKIS, S; VALSAMOPOULOS, P et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 9, pp 998-1003, issn 1552-4825, 6 p.Article

New Proposed Clinico-Radiologic and Molecular Criteria in Hypochondroplasia: FGFR 3 Gene Mutations Are Not the Only Cause of HypochondroplasiaSONG, Sang-Heon; ESTRERA BALCE, Gracia Cielo; VIKAS AGASHE, Mandar et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 10, pp 2456-2462, issn 1552-4825, 7 p.Article

Clinical hypochondroplasia in a family caused by a heterozygous double mutation in FGFR3 encoding GLY380LYSSANTOS, Heloisa G; ALMEIDA, Maria; FERNANDES, Helena et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 4, pp 355-359, issn 1552-4825, 5 p.Article

ASPETTI CLINICI E RADIOLOGICI DELL'IPOCONDROPLASIA. DESCRIZIONE DI SEI CASI = ASPECTS CLINIQUES ET RADIOLOGIQUES DE L'HYPOCHONDROPLASIE. DESCRIPTION DE 6 CASGEMME G; PINELLI G; BONIOLI E et al.1980; MINERVA PEDIATR.; ITA; DA. 1980; VOL. 32; NO 4; PP. 237-244; ABS. ENG; BIBL. 18 REF.Article

THE RADIOGRAPHIC MANIFESTATIONS OF HYPOCHONDROPLASIAHESELSON NG; CREMIN BJ; BEIGHTON P et al.1979; CLIN. RADIOL.; GBR; DA. 1979; VOL. 30; NO 1; PP. 79-85; BIBL. 14 REF.Article

HYPOCHONDROPLASIAGLASGOW JFT; NEVIN NC; THOMAS PS et al.1978; ARCH. DIS. CHILDH.; GBR; DA. 1978; VOL. 53; NO 11; PP. 868-872; BIBL. 12 REF.Article

Clinical and Molecular diagnosis of the skeletal dysplasias associated with mutations in the gene encoding Fibroblast Growth Factor Receptor 3 (FGFR3) in PortugalALMEIDA, M. R; CAMPOS-XAVIER, A. B; SOUSA, S et al.Clinical genetics. 2009, Vol 75, Num 2, pp 150-156, issn 0009-9163, 7 p.Article

FGFR3 Related Skeletal Dysplasias Diagnosed Prenatally by Ultrasonography and Molecular Analysis: Presentation of 17 CasesHATZAKI, Angeliki; SIFAKIS, Stavros; THEODOROPOULOS, Perikles et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 10, pp 2426-2435, issn 1552-4825, 10 p.Article

Prenatal diagnosis of hypochondroplasiaSTOLL, C; MANINI, P; BLOCH, J et al.Prenatal diagnosis. 1985, Vol 5, Num 6, pp 423-426, issn 0197-3851Article

Growth of children with hypochondroplasia treated with growth hormone for up to three yearsBRIDGES, N. A; HINDMARSH, P. C; BROOK, C. G. D et al.Hormone research. 1991, Vol 36, pp 56-60, issn 0301-0163, SUP1Conference Paper

Achondroplasia-hypochondroplasia complexSOMMER, A; YOUNG-WEE, T; FRYE, T et al.American journal of medical genetics. 1987, Vol 26, Num 4, pp 949-957, issn 0148-7299Article

Pitfall in diagnosing growth hormone deficiency in a hypochondroplastic patient with a delayed pubertyMEYER, M. F; MENKEN, K.-U; ZIMNY, S et al.Experimental and clinical endocrinology & diabetes. 2003, Vol 111, Num 3, pp 177-181, issn 0947-7349, 5 p.Article

Radiographic and genetic diagnosis of sporadic hypochondroplasia early in the neonatal periodKATAOKA, Soromon; SAWAI, Hideaki; YAMADA, Hideto et al.Prenatal diagnosis. 2004, Vol 24, Num 1, pp 45-49, issn 0197-3851, 5 p.Article

Douleur et psychisme. Sur la prise en charge de la douleur dans les maladies osseuses constitutionnelles = Pain and psyche. Concerning the handling of pain in constitutional bone diseasesPELLION, Tatiana.Evolution psychiatrique. 2014, Vol 79, Num 4, pp 767-779, issn 0014-3855, 13 p.Article

Hypochondroplasia and stature within normal limits: Another family with an Asn540Ser mutation in the fibroblast growth factor receptor 3 geneTHAUVIN-ROBINET, Christel; FAIVRE, Laurence; LEWIN, Patricia et al.American journal of medical genetics. 2003, Vol 119A, Num 1, pp 81-84, issn 0148-7299, 4 p.Article

Genotype phenotype correlation in achondroplasia and hypochondroplasiaMATSUI, Y; YASUI, N; KIMURA, T et al.Journal of bone and joint surgery. British volume. 1998, Vol 80, Num 6, pp 1052-1056, issn 0301-620XArticle

Common mutations in the fibroblast growth factor receptor 3 (FGFR 3) gene account for achondroplasia, hypochondroplasia, and thanatophoric dwarfismBONAVENTURE, J; ROUSSEAU, F; LEGEAI-MALLET, L et al.American journal of medical genetics. 1996, Vol 63, Num 1, pp 148-154, issn 0148-7299Article

A Pilot Study of Discontinuous, Insulin-Like Growth Factor 1―Dosing Growth Hormone Treatment in Young Children with FGFR3 N540K-Mutated HypochondroplasiaROTHENBUHLER, Anya; LINGLART, Agnès; PIQUARD, Catherine et al.The Journal of pediatrics. 2012, Vol 160, Num 5, pp 849-853, issn 0022-3476, 5 p.Article