Literature DB >> 10636995

Diagnostic dilemma caused by overlapping features of Prader-Willi syndrome and trisomy 18 during infancy.

H A Ishmael, L M Pasztor, P G Rothberg, M G Butler, J Pfotenhauer, V Hannig, M Summar.   

Abstract

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Year:  2000        PMID： 10636995      PMCID： PMC6800192          DOI： 10.1016/s0022-3476(00)90076-3

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


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  1 in total

1.  The neonatal presentation of Prader-Willi syndrome revisited.

Authors:  S P Miller; P Riley; M I Shevell
Journal:  J Pediatr       Date:  1999-02       Impact factor: 4.406
  1 in total
  1 in total

1.  Prader-Willi Syndrome: Clinical and Genetic Findings.

Authors:  Merlin G Butler; Travis Thompson
Journal:  Endocrinologist       Date:  2000-07
  1 in total

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