Literature DB >> 1121970

The Robinow syndrome: an isolated case with a detailed study of the phenotype.

T E Kelly, R Benson, S Temtamy, L Plotnick, S Levin.   

Abstract

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Year:  1975        PMID: 1121970     DOI: 10.1001/archpedi.1975.02120400081022

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


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  5 in total

1.  Robinow or "fetal face syndrome" in a male infant with ambiguous genitalia and androgen receptor deficiency.

Authors:  E Schönau; R A Pfeiffer; H U Schweikert; B Böwing; G Schott
Journal:  Eur J Pediatr       Date:  1990-06       Impact factor: 3.183

2.  Robinow syndrome with parental consanguinity.

Authors:  D Glaser; J Herbst; K Roggenkamp; W Tünte; W Lenz
Journal:  Eur J Pediatr       Date:  1989-06       Impact factor: 3.183

Review 3.  Robinow syndrome: report of two patients and review of literature.

Authors:  M G Butler; W B Wadlington
Journal:  Clin Genet       Date:  1987-02       Impact factor: 4.438

4.  Robinow syndrome: a diagnosis at the fingertips.

Authors:  Chaya N Murali; Beth Keena; Elaine H Zackai
Journal:  Clin Dysmorphol       Date:  2018-10       Impact factor: 0.816

5.  A new form of rhizo-mesomelic bone dysplasia.

Authors:  A Baxova; K Kozlowski; I Netriova
Journal:  Pediatr Radiol       Date:  1995
  5 in total

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