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5 in total

Review 1. Axenfeld-Rieger syndrome and spectrum of PITX2 and FOXC1 mutations.

Authors: Zeynep Tümer; Daniella Bach-Holm
Journal: Eur J Hum Genet Date: 2009-06-10 Impact factor: 4.246

2. Multiple congenital anomalies including the Rieger eye malformation in a boy with interstitial deletion of (4) (q25-->q27) secondary to a balanced insertion in his normal father: evidence for haplotype insufficiency causing the Rieger malformation.

Authors: A Schinzel; L Brecevic; F Dutly; A Baumer; F Binkert; R H Largo
Journal: J Med Genet Date: 1997-12 Impact factor: 6.318

Review 3. Toward the complete genomic map and molecular pathology of human chromosome 4.

Authors: O Riess; B Winkelmann; J T Epplen
Journal: Hum Genet Date: 1994-07 Impact factor: 4.132

4. A new case of an interstitial deletion (4)(q25q27) characterised by molecular cytogenetic techniques and review of the literature.

Authors: Sandra Anna Becker; Susanne Popp; Klaus Rager; Anna Jauch
Journal: Eur J Pediatr Date: 2003-02-19 Impact factor: 3.183

5. Renal Dysplasia and Progressive Renal Failure in a Newborn with Interstitial Chromosome 4 Deletion 4q25-28.3: A New Phenotype?

Authors: Cláudia Teles-Silva; Francisca Martins; Sandra Costa; Paulo Soares; Gustavo Rocha; Filipa Flor-de-Lima; Helena Pinto; Carla Ramalho; Renata Oliveira; Otília Brandão; Hercília Guimarães
Journal: J Pediatr Genet Date: 2020-01-22

5 in total