Literature DB >> 9863610

Kenny-Caffey syndrome without the CATCH 22 deletion.

T Yorifuji, J Muroi, A Uematsu.   

Abstract

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Year:  1998        PMID： 9863610      PMCID： PMC1051525          DOI： 10.1136/jmg.35.12.1054

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  5 in total

1.  Kenny-Caffey syndrome is part of the CATCH 22 haploinsufficiency cluster.

Authors:  M A Sabry; M Zaki; S J Abul Hassan; D G Ramadan; M A Abdel Rasool; S A al Awadi; Q al Saleh
Journal:  J Med Genet       Date:  1998-01       Impact factor: 6.318

2.  Kenny-Caffey syndrome in six Bedouin sibships: autosomal recessive inheritance is confirmed.

Authors:  K Tahseen; S Khan; R Uma; R Usha; M M Al Ghanem; S A Al Awadi; T I Farag
Journal:  Am J Med Genet       Date:  1997-03-17

3.  Dwarfism and cortical thickening of tubular bones. Transient hypocalcemia in a mother and son.

Authors:  F M Kenny; L Linarelli
Journal:  Am J Dis Child       Date:  1966-02

4.  Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variant.

Authors:  P Franceschini; A Testa; G Bogetti; E Girardo; A Guala; G Lopez-Bell; G Buzio; E Ferrario; E Piccato
Journal:  Am J Med Genet       Date:  1992-01-01

5.  The Kenny syndrome, a rare type of growth deficiency with tubular stenosis, transient hypoparathyroidism and anomalies of refraction.

Authors:  F Majewski; W Rosendahl; M Ranke; K Nolte
Journal:  Eur J Pediatr       Date:  1981-03       Impact factor: 3.183
  5 in total
  1 in total

Review 1.  Genetic causes of hypomagnesemia, a clinical overview.

Authors:  Daan H H M Viering; Jeroen H F de Baaij; Stephen B Walsh; Robert Kleta; Detlef Bockenhauer
Journal:  Pediatr Nephrol       Date:  2016-05-27       Impact factor: 3.714
  1 in total

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