Literature DB >> 5135852

Laurence-Moon-Biedl syndrome in presumably identical twins.

S Balci, B Say, R Erdal.   

Abstract

Mesh：

Year:  1971        PMID： 5135852     DOI： 10.1007/BF00273949

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  5 in total

1.  [CONTRIBUTION OF THE CLINICO-TWIN METHOD IN STUDY OF SEX ANOMALIES IN CHILDHOOD. (CASES OF TWINS WITH PHIMOSIS, HYPOSPADIAS, CRYPTORCHISM, HYPOPITUITARISM, ADIPOSO-GENITAL SYNDROME AND THE LAURENCE-MOON-BIEDL TYPE SYNDROME)].

Authors:  L GEDDA; F DIRAIMONDO
Journal:  Minerva Pediatr       Date:  1965-03-24       Impact factor: 1.312

2.  Laurence-Moon-Biedl syndrome in an Arab boy: familial incidence.

Authors:  V V KALBIAN
Journal:  J Clin Endocrinol Metab       Date:  1956-12       Impact factor: 5.958

3.  [Laurence-Moon-Biedl-Bardet syndrome in monozygotic twins; possible result of an intrauterine fetal injury].

Authors:  A MOENCH
Journal:  Z Geburtshilfe Gynakol       Date:  1954

4.  [Laurence-Moon-Bardot-Biedl syndrome. Apropos of 7 personal cases].

Authors:  M Bene; H Radu; M Kocsis; A Radu
Journal:  Ann Pediatr (Paris)       Date:  1969-01-02

5.  Four cases of "retinitis pigmentosa" occurring in the same family, and accompanied by general imperfections of development. 1866.

Authors:  J Z Laurence; R C Moon
Journal:  Obes Res       Date:  1995-07
  5 in total

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