Literature DB >> 8343920

Congenital trichomegaly, pigmentary degeneration of the retina and growth retardation (Oliver-McFarlane syndrome): 28-year follow-up of the first reported case.

T S Chang1, D C McFarlane, G Oliver, N R Willis.   

Abstract

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Year:  1993        PMID： 8343920

Source DB:  PubMed          Journal:  Can J Ophthalmol        ISSN： 0008-4182            Impact factor:   1.882


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  2 in total

1.  Congenital trichomegaly (Oliver-McFarlane syndrome): a case report with 9 years' follow up.

Authors:  C Haritoglou; G Rudolph; P Kalpadakis; K P Boergen
Journal:  Br J Ophthalmol       Date:  2003-01       Impact factor: 4.638

2.  Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromes.

Authors:  Robert B Hufnagel; Gavin Arno; Nichole D Hein; Joshua Hersheson; Megana Prasad; Yvonne Anderson; Laura A Krueger; Louise C Gregory; Corinne Stoetzel; Thomas J Jaworek; Sarah Hull; Abi Li; Vincent Plagnol; Christi M Willen; Thomas M Morgan; Cynthia A Prows; Rashmi S Hegde; Saima Riazuddin; Gregory A Grabowski; Rudy J Richardson; Klaus Dieterich; Taosheng Huang; Tamas Revesz; J P Martinez-Barbera; Robert A Sisk; Craig Jefferies; Henry Houlden; Mehul T Dattani; John K Fink; Helene Dollfus; Anthony T Moore; Zubair M Ahmed
Journal:  J Med Genet       Date:  2014-12-05       Impact factor: 6.318
  2 in total

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