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Review 1. Familial interruption of the aortic arch.

Authors: J W Gobel; M E Pierpont; J H Moller; A Singh; J E Edwards
Journal: Pediatr Cardiol Date: 1993-03 Impact factor: 1.655

Review 2. DiGeorge syndrome: an historical review of clinical and cytogenetic features.

Authors: F Greenberg
Journal: J Med Genet Date: 1993-10 Impact factor: 6.318

3. Successful pregnancies and reduced treatment requirement while breast feeding in a patient with congenital hypoparathyroidism due to homozygous c.68C>A null parathyroid hormone gene mutation.

Authors: Joanne Dixon; Steven Miller
Journal: BMJ Case Rep Date: 2018-05-26

4. 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

5. Unmasking of latent hypoparathyroidism in a child with partial DiGeorge syndrome by ethylenediaminetetraacetic acid infusion.

Authors: T Hasegawa; Y Hasegawa; T Yokoyama; S Koto; S Asamura; Y Tsuchiya
Journal: Eur J Pediatr Date: 1993-04 Impact factor: 3.183

Review 6. The DiGeorge anomaly.

Authors: R Hong
Journal: Clin Rev Allergy Immunol Date: 2001-02 Impact factor: 10.817

7. Endocrine and Growth Disorders in Taiwanese Children With 22q11.2 Deletion Syndrome.

Authors: Han-Yi Lin; Wen-Yu Tsai; Yi-Ching Tung; Shih-Yao Liu; Ni-Chung Lee; Yin-Hsiu Chien; Wuh-Liang Hwu; Cheng-Ting Lee
Journal: Front Endocrinol (Lausanne) Date: 2022-03-31 Impact factor: 5.555

7 in total