Literature DB >> 5173271

The Rud syndrome: ichthyosis, hypogonadism, mental retardation.

P S Nissley, G H Thomas.   

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Year:  1971        PMID： 5173271

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


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  3 in total

1.  An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometry.

Authors:  R E Schnur; B J Trask; G van den Engh; H H Punnett; M Kistenmacher; M A Tomeo; R E Naids; R L Nussbaum
Journal:  Am J Hum Genet       Date:  1989-11       Impact factor: 11.025

2.  Cryptorchidism and hypogenitalism in X-linked recessive ichthyosis vulgaris.

Authors:  H Traupe; H H Ropers
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

3.  Genetic heterogeneity of the ichthyosis, hypogonadism, mental retardation, and epilepsy syndrome. Clinical and biochemical investigations on two patients with Rud syndrome and review of the literature.

Authors:  M Münke; K Kruse; M Goos; H H Ropers; M Tolksdorf
Journal:  Eur J Pediatr       Date:  1983-10       Impact factor: 3.183
  3 in total

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