Literature DB >> 7158645

X-linked or autosomal dominant, lethal in the male, inheritance of the Melnick-Needles (osteodysplasty) syndrome? A reappraisal.

R J Gorlin, J Knier.   

Abstract

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Year:  1982        PMID： 7158645     DOI： 10.1002/ajmg.1320130417

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  6 in total

Review 1.  Frank-Ter Haar syndrome in a newborn.

Authors:  P Femitha; Rojo Joy; Bahubali D Gane; B Adhisivam; B Vishnu Bhat
Journal:  Indian J Pediatr       Date:  2011-10-29       Impact factor: 1.967

Review 2.  Melnick-Needles syndrome. Four new cases.

Authors:  K Eggli; M Giudici; J Ramer; J Easterbrook; J Madewell
Journal:  Pediatr Radiol       Date:  1992

3.  X-linked dominant inherited diseases with lethality in hemizygous males.

Authors:  R Wettke-Schäfer; G Kantner
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

4.  Serpentine fibula--polycystic kidney syndrome and Melnick-Needles syndrome are different disorders.

Authors:  F Majewski; H Enders; M B Ranke; T Voit
Journal:  Eur J Pediatr       Date:  1993-11       Impact factor: 3.183

5.  Congenital glaucoma as an ophthalmic manifestation of Frank-Ter Haar syndrome.

Authors:  Zeynep Aktas; Emine Esra Karaca; Nurcan Dogan; Tugba Çakmak; Metin Unlu; Levent Tok; Murat Hasanreisoglu
Journal:  Int Ophthalmol       Date:  2013-05-25       Impact factor: 2.031

6.  Melnick-Needles syndrome associated with growth hormone deficiency: a case report.

Authors:  Leyla Akın; Erdal Adal; Mustafa Ali Akın; Selim Kurtoğlu
Journal:  J Clin Res Pediatr Endocrinol       Date:  2009-08-07
  6 in total

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