Literature DB >> 1956068

The frequency of mental retardation in hypochondroplasia.

R Wynne-Davies, M A Patton.   

Abstract

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Year:  1991        PMID： 1956068      PMCID： PMC1015801          DOI： 10.1136/jmg.28.9.644

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  2 in total

1.  The genetic entity of hypochondroplasia.

Authors:  M Frydman; M Hertz; R M Goodman
Journal:  Clin Genet       Date:  1974       Impact factor: 4.438

2.  Hypochondroplasia: clinical and radiological aspects in 39 cases.

Authors:  B D Hall; J Spranger
Journal:  Radiology       Date:  1979-10       Impact factor: 11.105
  2 in total
  2 in total

1.  Clinical management and emerging therapies of FGFR3-related skeletal dysplasia in childhood.

Authors:  Hwa Young Kim; Jung Min Ko
Journal:  Ann Pediatr Endocrinol Metab       Date:  2022-06-30

2.  Hypochondroplasia in a child with 1620C>G (Asn540Lys) mutation in FGFR3.

Authors:  Hüseyin Anıl Korkmaz; Filiz Hazan; Ceyhun Dizdarer; Ajlan Tükün
Journal:  J Clin Res Pediatr Endocrinol       Date:  2012-11-12
  2 in total

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