Literature DB >> 5948041

Congenital heart disease, deaf-mutism and associated somatic malformations occurring in several members of one family.

G T Koroxenidis, N C Webb, C B Moschos, P H Lehan.   

Abstract

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Year:  1966        PMID: 5948041     DOI: 10.1016/0002-9343(66)90196-3

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


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  7 in total

1.  Multiple lentigines syndrome (LEOPARD syndrome or progressive cardiomyopathic lentiginosis).

Authors:  B D Coppin; I K Temple
Journal:  J Med Genet       Date:  1997-07       Impact factor: 6.318

2.  The heart in lentiginosis.

Authors:  J Somerville; R E Bonham-Carter
Journal:  Br Heart J       Date:  1972-01

3.  Pulmonary valvular dysplasia. A cardiofacial syndrome.

Authors:  L M Linde; S W Turner; R S Sparkes
Journal:  Br Heart J       Date:  1973-03

Review 4.  Inherited diseases of the inner ear in man in the light of studies on the mouse.

Authors:  M S Deol
Journal:  J Med Genet       Date:  1968-06       Impact factor: 6.318

5.  Premature cataracts associated with generalized lentigo.

Authors:  R O Howard
Journal:  Trans Am Ophthalmol Soc       Date:  1979

6.  Cardio-auditory syndromes. Cardiac and genetic study of 511 deaf-mute children.

Authors:  A Sánchez Cascos; L Sánchez-Harguindey; P De Rábago
Journal:  Br Heart J       Date:  1969-01

7.  'Little leopard' syndrome. Description of 3 cases and review of 24.

Authors:  D Pickering; B Laski; D C Macmillan; V Rose
Journal:  Arch Dis Child       Date:  1971-02       Impact factor: 3.791

  7 in total

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