Literature DB >> 1583661

Weaver syndrome.

T R Cole1, N R Dennis, H E Hughes.   

Abstract

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Year:  1992        PMID： 1583661      PMCID： PMC1015954          DOI： 10.1136/jmg.29.5.332

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  24 in total

Review 1.  A comprehensive and critical assessment of overgrowth and overgrowth syndromes.

Authors:  M M Cohen
Journal:  Adv Hum Genet       Date:  1989

2.  Psychological characteristics of Sotos syndrome.

Authors:  S C Rutter; T R Cole
Journal:  Dev Med Child Neurol       Date:  1991-10       Impact factor: 5.449

3.  A new autosomal recessive disorder resembling Weaver syndrome.

Authors:  A S Teebi; T S Sundareshan; M Y Hammouri; S A al-Awadi; Q A al-Saleh
Journal:  Am J Med Genet       Date:  1989-08

4.  Letter: Optimal antibiotic and antitoxin treatment of tetanus?

Authors:  J W Bass
Journal:  J Pediatr       Date:  1974-10       Impact factor: 4.406

5.  Update on the Marshall-Smith-Weaver controversy.

Authors:  N Fitch
Journal:  Am J Med Genet       Date:  1985-03

6.  Weaver syndrome with pes cavus.

Authors:  S A Farrell; H E Hughes
Journal:  Am J Med Genet       Date:  1985-08

7.  A Weaver-like syndrome with endocrinological abnormalities in a boy and his mother.

Authors:  C Stoll; P Talon; L Mengus; M P Roth; B Dott
Journal:  Clin Genet       Date:  1985-09       Impact factor: 4.438

8.  A girl with the Weaver syndrome.

Authors:  E M Thompson; S Hill; J V Leonard; M E Pembrey
Journal:  J Med Genet       Date:  1987-04       Impact factor: 6.318

9.  Weaver syndrome: the changing phenotype in an adult.

Authors:  F Greenberg; W Wasiewski; E R McCabe
Journal:  Am J Med Genet       Date:  1989-05

10.  Weaver-Smith syndrome. A case study with long-term follow-up.

Authors:  N Amir; E Gross-Kieselstein; H J Hirsch; E Lax; R Silverberg-Shalev
Journal:  Am J Dis Child       Date:  1984-12
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  10 in total

1.  NSD1 mutations are the major cause of Sotos syndrome and occur in some cases of Weaver syndrome but are rare in other overgrowth phenotypes.

Authors:  Jenny Douglas; Sandra Hanks; I Karen Temple; Sally Davies; Alexandra Murray; Meena Upadhyaya; Susan Tomkins; Helen E Hughes; Trevor R P Cole; Nazneen Rahman
Journal:  Am J Hum Genet       Date:  2002-12-02       Impact factor: 11.025

2.  Sotos syndrome: a study of the diagnostic criteria and natural history.

Authors:  T R Cole; H E Hughes
Journal:  J Med Genet       Date:  1994-01       Impact factor: 6.318

3.  Autosomal dominant inheritance of Weaver syndrome.

Authors:  A Fryer; C Smith; L Rosenbloom; T Cole
Journal:  J Med Genet       Date:  1997-05       Impact factor: 6.318

4.  Familial neurofibromatosis type 1 associated with an overgrowth syndrome resembling Weaver syndrome.

Authors:  C J van Asperen; W C Overweg-Plandsoen; M H Cnossen; D A van Tijn; R C Hennekam
Journal:  J Med Genet       Date:  1998-04       Impact factor: 6.318

5.  Specific entities affecting the craniocervical region: syndromes affecting the craniocervical junction.

Authors:  Arnold H Menezes; Timothy W Vogel
Journal:  Childs Nerv Syst       Date:  2008-03-28       Impact factor: 1.475

6.  Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height.

Authors:  Katrina Tatton-Brown; Sandra Hanks; Elise Ruark; Anna Zachariou; Silvana Del Vecchio Duarte; Emma Ramsay; Katie Snape; Anne Murray; Elizabeth R Perdeaux; Sheila Seal; Chey Loveday; Siddharth Banka; Carol Clericuzio; Frances Flinter; Alex Magee; Vivienne McConnell; Michael Patton; Wolfgang Raith; Julia Rankin; Miranda Splitt; Volker Strenger; Clare Taylor; Patricia Wheeler; Karen I Temple; Trevor Cole; Jenny Douglas; Nazneen Rahman
Journal:  Oncotarget       Date:  2011-12

7.  Histone code, human growth and cancer.

Authors:  Francesco Crea
Journal:  Oncotarget       Date:  2012-01

8.  Hormonal and genetical assessment of a Japanese girl with weaver syndrome.

Authors:  Yoko Miyoshi; Masako Taniike; Ikuko Mohri; Sotaro Mushiake; Shigeo Nakajima; Naomichi Matsumoto; Keiichi Ozono
Journal:  Clin Pediatr Endocrinol       Date:  2004-07-07

Review 9.  New Insights into the Control of Cell Fate Choices and Differentiation by Retinoic Acid in Cranial, Axial and Caudal Structures.

Authors:  Heidrun Draut; Thomas Liebenstein; Gerrit Begemann
Journal:  Biomolecules       Date:  2019-12-11

Review 10.  Overgrowth Syndromes-Evaluation, Diagnosis, and Management.

Authors:  Joshua Manor; Seema R Lalani
Journal:  Front Pediatr       Date:  2020-10-30       Impact factor: 3.418
  10 in total

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