Literature DB >> 2515374

Dermatoglyphic study in children with phenylketonuria.

S Balci1, F Tanzer, M Atasu, I Ozalp.   

Abstract

Dermatoglyphic findings in 19 patients with phenylketonuria (11 male and 8 female), 39 of their relatives (18 female and 21 male) and 500 controls (TRC) were not statistically significant among the three groups studied. There was no definite relationship between the phenylketonuric gene and the dermatoglyphic patterns. The parents of half the phenylketonuria cases are not consanguineous; thus the phenylketonuria gene may be more frequent in Turkey than other European countries.

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Year:  1989        PMID: 2515374     DOI: 10.1007/bf01799225

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  5 in total

1.  Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world: a collaborative study.

Authors: 
Journal:  Humangenetik       Date:  1975-12-23

2.  An information and discriminant analysis of fingerprint patterns pertaining to identification of mongolism and mental retardation.

Authors:  K H Lu
Journal:  Am J Hum Genet       Date:  1968-01       Impact factor: 11.025

3.  The genesis of dermatoglyphics.

Authors:  J J Mulvihill; D W Smith
Journal:  J Pediatr       Date:  1969-10       Impact factor: 4.406

4.  Dermatoglyphic nomogram for the diagnosis of Down's syndrome.

Authors:  T E Reed; D S Borgaonkar; P M Conneally; P Yu; W E Nance; J C Christian
Journal:  J Pediatr       Date:  1970-12       Impact factor: 4.406

5.  Finger, hand and foot prints in phenylketonuria as compared with other normal and abnormal populations.

Authors:  W Hirsch
Journal:  Humangenetik       Date:  1965
  5 in total

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