Literature DB >> 6737144

Smith-Lemli-Opitz syndrome and Hirschsprung disease.

A Lipson, A Hayes.   

Abstract

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Year:  1984        PMID： 6737144     DOI： 10.1016/s0022-3476(84)80406-0

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


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  5 in total

1.  Behaviour disorder in monosomy 10qter.

Authors:  L Mehta; D P Duckett; I D Young
Journal:  J Med Genet       Date:  1987-03       Impact factor: 6.318

2.  Surgical implications of the Smith-Lemli-Opitz syndrome.

Authors:  R J Craigie; M Ba'ath; A Fryer; C Baillie
Journal:  Pediatr Surg Int       Date:  2005-04-15       Impact factor: 1.827

3.  Normal cognition and behavior in a Smith-Lemli-Opitz syndrome patient who presented with Hirschsprung disease.

Authors:  C Mueller; S Patel; M Irons; K Antshel; G Salen; G S Tint; C Bay
Journal:  Am J Med Genet A       Date:  2003-11-15       Impact factor: 2.802

4.  The lethal multiple congenital anomaly syndrome of polydactyly, sex reversal, renal hypoplasia, and unilobular lungs.

Authors:  D Donnai; I D Young; W G Owen; S A Clark; P F Miller; W F Knox
Journal:  J Med Genet       Date:  1986-02       Impact factor: 6.318

Review 5.  Lethal acrodysgenital dwarfism: a severe lethal condition resembling Smith-Lemli-Opitz syndrome.

Authors:  M L Merrer; M L Briard; S Girard; N Mulliez; C Moraine; M C Imbert
Journal:  J Med Genet       Date:  1988-02       Impact factor: 6.318
  5 in total

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