Literature DB >> 14201663

BRACHMANN/DE LANGE SYNDROME.

J M OPITZ, A T SEGAL, R LEHRKE, H NADLER.   

Abstract

Keywords:  ABNORMALITIES; BRAIN DISEASES; CHROMOSOME ABNORMALITIES; DIAGNOSIS; INFANT; MENTAL RETARDATION; MUSCULAR DISEASES

Mesh:

Year:  1964        PMID: 14201663     DOI: 10.1016/s0140-6736(64)90980-8

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


× No keyword cloud information.
  8 in total

Review 1.  Dominant paternal transmission of Cornelia de Lange syndrome: a new case and review of 25 previously reported familial recurrences.

Authors:  K L Russell; J E Ming; K Patel; L Jukofsky; M Magnusson; I D Krantz
Journal:  Am J Med Genet       Date:  2001-12-15

2.  A case of Cornelia de Lange's syndrome.

Authors:  B W McGuinness
Journal:  J Coll Gen Pract       Date:  1967-03

3.  de Lange syndrome (Amsterdam dwarfism).

Authors:  D M MacDonald
Journal:  Proc R Soc Med       Date:  1973-12

4.  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

5.  Cornelia de Lange syndrome in several members of the same family.

Authors:  D Kumar; C E Blank; B L Griffiths
Journal:  J Med Genet       Date:  1985-08       Impact factor: 6.318

6.  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

7.  Self-inflicted corneal injuries in children with congenital corneal anaesthesia.

Authors:  G E Trope; J L Jay; J Dudgeon; G Woodruff
Journal:  Br J Ophthalmol       Date:  1985-07       Impact factor: 4.638

8.  The Cornelia de Lange syndrome: clinical and cytogenetic interpretations.

Authors:  H W Payne; W K Maeda
Journal:  Can Med Assoc J       Date:  1965-09-11       Impact factor: 8.262

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.