Literature DB >> 9613346

Growing interest in overgrowth.

T Cole1.   

Abstract

Mesh：

Year:  1998        PMID： 9613346      PMCID： PMC1717479          DOI： 10.1136/adc.78.3.200

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  33 in total

1.  CEREBRAL GIGANTISM IN CHILDHOOD. A SYNDROME OF EXCESSIVELY RAPID GROWTH AND ACROMEGALIC FEATURES AND A NONPROGRESSIVE NEUROLOGIC DISORDER.

Authors:  J F SOTOS; P R DODGE; D MUIRHEAD; J D CRAWFORD; N B TALBOT
Journal:  N Engl J Med       Date:  1964-07-16       Impact factor: 91.245

2.  Craniofacial syndromes: no such thing as a single gene disease.

Authors:  J J Mulvihill
Journal:  Nat Genet       Date:  1995-02       Impact factor: 38.330

3.  Glypicans: a growing trend.

Authors:  R Weksberg; J A Squire; D M Templeton
Journal:  Nat Genet       Date:  1996-03       Impact factor: 38.330

4.  Clinical features and natural history of Beckwith-Wiedemann syndrome: presentation of 74 new cases.

Authors:  M Elliott; R Bayly; T Cole; I K Temple; E R Maher
Journal:  Clin Genet       Date:  1994-08       Impact factor: 4.438

5.  Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome.

Authors:  G Pilia; R M Hughes-Benzie; A MacKenzie; P Baybayan; E Y Chen; R Huber; G Neri; A Cao; A Forabosco; D Schlessinger
Journal:  Nat Genet       Date:  1996-03       Impact factor: 38.330

6.  Adrenocorticotropin receptor gene mutations in familial glucocorticoid deficiency: relationships with clinical features in four families.

Authors:  A Weber; J Toppari; R D Harvey; R C Klann; N J Shaw; A T Ricker; K Näntö-Salonen; J S Bevan; A J Clark
Journal:  J Clin Endocrinol Metab       Date:  1995-01       Impact factor: 5.958

7.  Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia.

Authors:  M Mannens; J M Hoovers; E Redeker; M Verjaal; A P Feinberg; P Little; M Boavida; N Coad; M Steenman; J Bliek
Journal:  Eur J Hum Genet       Date:  1994       Impact factor: 4.246

8.  Mutation in fibrillin-1 and the Marfanoid-craniosynostosis (Shprintzen-Goldberg) syndrome.

Authors:  S Sood; Z A Eldadah; W L Krause; I McIntosh; H C Dietz
Journal:  Nat Genet       Date:  1996-02       Impact factor: 38.330

9.  Somatic overgrowth associated with overexpression of insulin-like growth factor II.

Authors:  I M Morison; D M Becroft; T Taniguchi; C G Woods; A E Reeve
Journal:  Nat Med       Date:  1996-03       Impact factor: 53.440

10.  Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, congenital contractural arachnodactyly.

Authors:  E A Putnam; H Zhang; F Ramirez; D M Milewicz
Journal:  Nat Genet       Date:  1995-12       Impact factor: 38.330
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  3 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, failure to thrive and parotitis.

Authors:  Megan R Thomas
Journal:  BMJ Case Rep       Date:  2011-03-01

3.  Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter.

Authors:  Marie Sogaard; Zeynep Tümer; Helle Hjalgrim; Johanne Hahnemann; Birgitte Friis; Paal Ledaal; Vibeke Faurholt Pedersen; Peter Baekgaard; Niels Tommerup; Sultan Cingöz; Morten Duno; Karen Brondum-Nielsen
Journal:  BMC Med Genet       Date:  2005-05-17       Impact factor: 2.103
  3 in total

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