Literature DB >> 974247

Familial thymic aplasia with intrauterine growth retardation and fetal death: a new syndrome or a variant of DiGeorge syndrome.

M K Shepard, S K Linman, A Cavazos.   

Abstract

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Year:  1976        PMID： 974247

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


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  6 in total

1.  Facial dysmorphia, parathyroid and thymic dysfunction in the father of a newborn with the DiGeorge complex.

Authors:  P D Maaswinkel-Mooij; S E Papapoulos; E J Gerritsen; A H Mudde; J J Van de Kamp
Journal:  Eur J Pediatr       Date:  1989-12       Impact factor: 3.183

2.  A deletion in chromosome 22 can cause DiGeorge syndrome.

Authors:  A de la Chapelle; R Herva; M Koivisto; P Aula
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

3.  Errors of morphogenesis and inborn errors of immunity 20 years after the discovery of DiGeorge anomaly.

Authors:  G R Burgio; A G Ugazio
Journal:  Eur J Pediatr       Date:  1985-05       Impact factor: 3.183

Review 4.  Human chromosome 22.

Authors:  J C Kaplan; A Aurias; C Julier; M Prieur; M F Szajnert
Journal:  J Med Genet       Date:  1987-02       Impact factor: 6.318

5.  Familial DiGeorge syndrome with tetralogy of Fallot and prolonged survival.

Authors:  W E Winter; J H Silverstein; D J Barrett; E Kiel
Journal:  Eur J Pediatr       Date:  1984-01       Impact factor: 3.183

6.  Cardiovascular malformations in DiGeorge syndrome (congenital absence of hypoplasia of the thymus).

Authors:  P Moerman; P Goddeeris; J Lauwerijns; L G Van der Hauwaert
Journal:  Br Heart J       Date:  1980-10
  6 in total

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