Literature DB >> 14261013

THE DE LANGE SYNDROME.

Z H HART, R I JASLOW, M R GOMEZ.   

Abstract

Keywords:  ABNORMALITIES; BLOOD ALKALINE PHOSPHATASE; CHILD; CHROMOSOMES; DIAGNOSIS; ELECTROLYTES; FACIAL EXPRESSION; FOOT DISEASES; HAND DEFORMITIES; HIRSUTISM; HYPERTRICHOSIS; MENTAL RETARDATION; METABOLISM; NITROGEN; THYROID GLAND FUNCTION TESTS

Mesh:

Substances:

Year:  1965        PMID: 14261013     DOI: 10.1001/archpedi.1965.02090020327012

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


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  5 in total

Review 1.  Causes of death and autopsy findings in a large study cohort of individuals with Cornelia de Lange syndrome and review of the literature.

Authors:  Samantha A Schrier; Ilana Sherer; Matthew A Deardorff; Dinah Clark; Lynn Audette; Lynette Gillis; Antonie D Kline; Linda Ernst; Kathleen Loomes; Ian D Krantz; Laird G Jackson
Journal:  Am J Med Genet A       Date:  2011-11-08       Impact factor: 2.802

2.  Cornelia de lange syndrome. Report of 2 cases in siblings.

Authors:  V N Ingle; V B Mali
Journal:  Indian J Pediatr       Date:  1970-04       Impact factor: 1.967

3.  De Lange syndrome: report of 20 cases.

Authors:  R G McArthur; J H Edwards
Journal:  Can Med Assoc J       Date:  1967-04-29       Impact factor: 8.262

Review 4.  Cecal volvulus in children with mental disability.

Authors:  Kohei Takada; Yoshinori Hamada; Masato Sato; Yoshimitsu Fujii; Masayuki Teraguchi; Kazumari Kaneko; Yasuo Kamiyama
Journal:  Pediatr Surg Int       Date:  2007-10       Impact factor: 1.827

Review 5.  Integrating molecular and structural findings: Wnt as a possible actor in shaping cognitive impairment in Cornelia de Lange syndrome.

Authors:  Laura Avagliano; Paolo Grazioli; Milena Mariani; Gaetano P Bulfamante; Angelo Selicorni; Valentina Massa
Journal:  Orphanet J Rare Dis       Date:  2017-11-21       Impact factor: 4.123

  5 in total

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