Literature DB >> 1682750

Antenatal diagnosis of DiGeorge syndrome.

D A Driscoll, M L Budarf, B S Emanuel.   

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Year:  1991        PMID： 1682750     DOI： 10.1016/0140-6736(91)92264-3

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


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  6 in total

1.  A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

Authors:  D A Driscoll; M L Budarf; B S Emanuel
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

2.  22q11 microdeletion studies in the heart tissue of an abortus involving a familial form of congenital heart disease.

Authors:  Z M Patel; H M Gawde; M I Khatkhatay
Journal:  J Clin Lab Anal       Date:  2006       Impact factor: 2.352

3.  Recurrence of DiGeorge syndrome: prenatal detection by FISH of a molecular 22q11 deletion.

Authors:  J O Van Hemel; C Schaap; D Van Opstal; M P Mulder; M F Niermeijer; J H Meijers
Journal:  J Med Genet       Date:  1995-08       Impact factor: 6.318

4.  Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.

Authors:  D A Driscoll; J Salvin; B Sellinger; M L Budarf; D M McDonald-McGinn; E H Zackai; B S Emanuel
Journal:  J Med Genet       Date:  1993-10       Impact factor: 6.318

5.  Prediction, prevention and personalisation of medication for the prenatal period: genetic prenatal tests for both rare and common diseases.

Authors:  Munis Dundar; Asli Subasioglu Uzak; Murat Erdogan; Yagut Akbarova
Journal:  EPMA J       Date:  2011-05-06       Impact factor: 6.543

6.  Variety of prenatally diagnosed congenital heart disease in 22q11.2 deletion syndrome.

Authors:  Mi-Young Lee; Hye-Sung Won; Ju Won Baek; Jae-Hyun Cho; Jae-Yoon Shim; Pil-Ryang Lee; Ahm Kim
Journal:  Obstet Gynecol Sci       Date:  2014-01-16
  6 in total

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