Literature DB >> 4214375

Autosomal dominant transmission of isolated growth hormone deficiency in iris-dental dysplasia (Rieger's syndrome).

A Sadeghi-Nejad, B Senior.   

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Year:  1974        PMID: 4214375     DOI: 10.1016/s0022-3476(74)80507-x

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


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  8 in total

1.  The Axenfeld syndrome and the Rieger syndrome.

Authors:  N Fitch; M Kaback
Journal:  J Med Genet       Date:  1978-02       Impact factor: 6.318

2.  Axenfeld-Rieger syndrome: a theory of mechanism and distinctions from the iridocorneal endothelial syndrome.

Authors:  M B Shields
Journal:  Trans Am Ophthalmol Soc       Date:  1983

Review 3.  Stunted growth with more or less normal appearance.

Authors:  J R Bierich; H Enders; U Heinrich; R Huenges; M B Ranke; D Schoenberg
Journal:  Eur J Pediatr       Date:  1982-12       Impact factor: 3.183

Review 4.  Molecular defects in the growth hormone-IGF axis.

Authors:  Joyce Lee; Ram K Menon
Journal:  Indian J Pediatr       Date:  2005-02       Impact factor: 1.967

5.  Microphthalmia with single central incisor and hypopituitarism.

Authors:  H G Artman; E Boyden
Journal:  J Med Genet       Date:  1990-03       Impact factor: 6.318

6.  Aetiology of idiopathic growth hormone deficiency in England and Wales.

Authors:  R J Rona; J M Tanner
Journal:  Arch Dis Child       Date:  1977-03       Impact factor: 3.791

7.  Recessively inherited growth hormone deficiency in a family from Iraq.

Authors:  M D Donaldson; S M Tucker; D B Grant
Journal:  J Med Genet       Date:  1980-08       Impact factor: 6.318

8.  Mutational analysis of the PITX2 coding region revealed no common cause for transposition of the great arteries (dTGA).

Authors:  Nadja Muncke; Beate Niesler; Ralph Roeth; Karin Schön; Heinz-Juergen Rüdiger; Elizabeth Goldmuntz; Judith Goodship; Gudrun Rappold
Journal:  BMC Med Genet       Date:  2005-05-12       Impact factor: 2.103

  8 in total

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