DiGeorge syndrome: an historical review of clinical and cytogenetic features.

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

22 citing papers in PubMed.

1. Clinical and genetic characterization of patients with Digeorge syndrome: a single-center, first report from Sudan.BMC pediatrics · 2026
   Article
2. Recent Advancements in Regenerative Approaches for Thymus Rejuvenation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
   Review
3. Self-organizing neuruloids model developmental aspects of Huntington's disease in the ectodermal compartment.Nature biotechnology · 2019
   Article
4. Immune and Genetic Features of the Chromosome 22q11.2 Deletion (DiGeorge Syndrome).Current allergy and asthma reports · 2018
   Review
5. Engineering approaches for regeneration of T lymphopoiesis.Biomaterials research · 2016
   Review
6. How insights from cardiovascular developmental biology have impacted the care of infants and children with congenital heart disease.Mechanisms of development · 2012
   Review
7. [Genetic causes in mild speech acquisition delay with/without mild developmental delay: significance for ENT physicians].HNO · 2010
   Article
8. The DiGeorge anomaly.Clinical reviews in allergy & immunology · 2001
   Review
9. 22q11 deletion syndrome: a genetic subtype of schizophrenia.Biological psychiatry · 1999
   Review
10. Velocardiofacial syndrome.Postgraduate medical journal · 1997
    Review
11. Features of DiGeorge syndrome and CHARGE association in five patients.Journal of medical genetics · 1997
    Article
12. Isomerism of the atrial appendages associated with 22q11 deletion in a fetus.Heart (British Cardiac Society) · 1996
    Article
13. Two sibs with Wolf-Hirschhorn and DiGeorge deletions resulting from an unbalanced chromosome rearrangement, 45,XX/XY, der(4)t(4;22) (p16.3;q11.2) mat,-22.Journal of medical genetics · 1996
    Article
14. How many breaks do we need to CATCH on 22q11?American journal of human genetics · 1996
    Review
15. Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome.American journal of human genetics · 1996
    Article
16. Recurrence of DiGeorge syndrome: prenatal detection by FISH of a molecular 22q11 deletion.Journal of medical genetics · 1995
    Article
17. 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot.Human genetics · 1995
    Article
18. Clinical and molecular study of DiGeorge sequence.European journal of pediatrics · 1994
    Article
19. A newborn with ring chromosome 10, aganglionic megacolon, and renal hypoplasia.Journal of medical genetics · 1994
    Article
20. "CATCH 22" sans cardiac anomaly, thymic hypoplasia, cleft palate, and hypocalcaemia: cAtch 22. A common result of 22q11 deficiency?Journal of medical genetics · 1994
    Article

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

Authors and funding

1 author.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

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