Literature DB >> 4959856

A new oculocerebral syndrome with hypopigmentation.

H E Cross, V A McKusick, W Breen.   

Abstract

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Year:  1967        PMID: 4959856     DOI: 10.1016/s0022-3476(67)80137-9

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


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  10 in total

1.  Oculocutaneous albinism accompanied by minor morphologic stigmata and reduced number and function of NK cells. A new variant of NK cell defect?

Authors:  Susanne Reich; Rolf Keitzer; Reinhold E Schmidt; Roland Jacobs; Verena Varnholt; Dietke Buck; Ralf Herold; Harald Renz
Journal:  Eur J Pediatr       Date:  2008-01-17       Impact factor: 3.183

2.  An oculocerebral hypopigmentation syndrome: a case report with clinical, histochemical, and ultrastructural findings.

Authors:  M A Patton; M Baraitser; A H Heagerty; R A Eady
Journal:  J Med Genet       Date:  1987-02       Impact factor: 6.318

3.  Amish albinism: a distinctive autosomal recessive phenotype.

Authors:  W E Nance; C E Jackson; C J Witkop
Journal:  Am J Hum Genet       Date:  1970-09       Impact factor: 11.025

4.  Corneal clouding, subvalvular aortic stenosis, and midfacial hypoplasia associated with mental deficiency and growth retardation--a new syndrome?

Authors:  J P Fryns; H Van den Berghe
Journal:  Eur J Pediatr       Date:  1979-06-28       Impact factor: 3.183

5.  Primary mesodermal dysgenesis of the cornea (Peters' anomaly) in two brothers.

Authors:  M Boel; J Timmermans; L Emmery; G Dralands; J P Fryns; H Van den Berghe
Journal:  Hum Genet       Date:  1979-10-01       Impact factor: 4.132

6.  Keratoconus posticus circumscriptus, cleft lip and palate, genitourinary abnormalities, short stature, and mental retardation in sibs.

Authors:  I D Young; W G Macrae; H E Hughes; J S Crawford
Journal:  J Med Genet       Date:  1982-10       Impact factor: 6.318

7.  Spastic paraplegia, optic atrophy, microcephaly with normal intelligence, and XY sex reversal: a new autosomal recessive syndrome?

Authors:  A S Teebi; S Miller; H Ostrer; P Eydoux; C Colomb-Brockmann; K Oudjhane; G Watters
Journal:  J Med Genet       Date:  1998-09       Impact factor: 6.318

8.  Disordered pigmentation, spastic paraparesis and peripheral neuropathy in three siblings: a new neurocutaneous syndrome.

Authors:  A Abdallat; S M Davis; J Farrage; W I McDonald
Journal:  J Neurol Neurosurg Psychiatry       Date:  1980-11       Impact factor: 10.154

Review 9.  Genetics of microphthalmos.

Authors:  M Warburg
Journal:  Int Ophthalmol       Date:  1981-08       Impact factor: 2.031

10.  Long term follow up of idiopathic gingival enlargement associated with chronic periodontitis: A case report and review.

Authors:  Girish P Nagarale; S Ravindra; Srinath Thakur; Swati Setty
Journal:  J Indian Soc Periodontol       Date:  2013-03
  10 in total

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