Literature DB >> 4156651

Dwarfism and congenital medullary stenosis (Kenny syndrome).

M G Wilson, R F Maronde, V G Mikity, N W Shinno.   

Abstract

Entities:  

Mesh:

Year:  1974        PMID: 4156651

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


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  3 in total

1.  FAM111A mutations result in hypoparathyroidism and impaired skeletal development.

Authors:  Sheila Unger; Maria W Górna; Antony Le Béchec; Sonia Do Vale-Pereira; Maria Francesca Bedeschi; Stefan Geiberger; Giedre Grigelioniene; Eva Horemuzova; Faustina Lalatta; Ekkehart Lausch; Cinzia Magnani; Sheela Nampoothiri; Gen Nishimura; Duccio Petrella; Francisca Rojas-Ringeling; Akari Utsunomiya; Bernhard Zabel; Sylvain Pradervand; Keith Harshman; Belinda Campos-Xavier; Luisa Bonafé; Giulio Superti-Furga; Brian Stevenson; Andrea Superti-Furga
Journal:  Am J Hum Genet       Date:  2013-05-16       Impact factor: 11.025

2.  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

3.  Oral rehabilitation of a patient with Kenny-Caffey syndrome using telescopic overdenture.

Authors:  Abu Nazar; Roshy George; Nicholas Mathew
Journal:  J Indian Prosthodont Soc       Date:  2021 Apr-Jun
  3 in total

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