Literature DB >> 14968319

[Child language development delay in craniofacial dysplasia].

C Schwemmle1, K Lüerssen, R Tolloczko, M Ptok.   

Abstract

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Year:  2004        PMID： 14968319     DOI： 10.1007/s00106-003-0919-6

Source DB:  PubMed          Journal:  HNO        ISSN： 0017-6192            Impact factor:   1.284


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  10 in total

1.  Construction of a detailed physical and transcript map of the candidate region for Russell-Silver syndrome on chromosome 17q23-q24.

Authors:  S Dörr; A T Midro; C Färber; J Giannakudis; I Hansmann
Journal:  Genomics       Date:  2001-01-15       Impact factor: 5.736

2.  Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy.

Authors:  T Eggermann; H A Wollmann; R Kuner; K Eggermann; H Enders; P Kaiser; M B Ranke
Journal:  Hum Genet       Date:  1997-09       Impact factor: 4.132

3.  A syndrome of intra-uterine dwarfism recognizable at birth with cranio-facial dysostosis, disproportionately short arms, and other anomalies (5 examples).

Authors:  A RUSSELL
Journal:  Proc R Soc Med       Date:  1954-12

4.  Syndrome of congenital hemihypertrophy, shortness of stature, and elevated urinary gonadotropins.

Authors:  H K SILVER; W KIYASU; J GEORGE; W C DEAMER
Journal:  Pediatrics       Date:  1953-10       Impact factor: 7.124

5.  The natural history of the Silver-Russell syndrome: a longitudinal study of thirty-nine cases.

Authors:  J M Tanner; H Lejarraga; N Cameron
Journal:  Pediatr Res       Date:  1975-08       Impact factor: 3.756

Review 6.  Three-generation dominant transmission of the Silver-Russell syndrome.

Authors:  P A Duncan; J G Hall; L R Shapiro; B K Vibert
Journal:  Am J Med Genet       Date:  1990-02

7.  Autosomal dominant Russell-Silver syndrome.

Authors:  S Al-Fifi; A S Teebi; M Shevell
Journal:  Am J Med Genet       Date:  1996-01-02

8.  The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria.

Authors:  S M Price; R Stanhope; C Garrett; M A Preece; R C Trembath
Journal:  J Med Genet       Date:  1999-11       Impact factor: 6.318

9.  Phenotypic and genetic analysis of the silver-Russell syndrome.

Authors:  V Escobar; S Gleiser; D D Weaver
Journal:  Clin Genet       Date:  1978-03       Impact factor: 4.438

10.  Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndrome.

Authors:  C A Joyce; A Sharp; J M Walker; H Bullman; I K Temple
Journal:  Hum Genet       Date:  1999-09       Impact factor: 4.132
  10 in total

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