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5 in total

1. A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndrome.

Authors: R D Jefferson; J Burn; K L Gaunt; S Hunter; E V Davison
Journal: J Med Genet Date: 1986-10 Impact factor: 6.318

2. Interstitial deletion of chromosome 4q diagnosed prenatally.

Authors: J M Campbell; J Williams; G Batcup
Journal: J Med Genet Date: 1986-08 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

Review 4. Genetic factors in congenital diaphragmatic hernia.

Authors: A M Holder; M Klaassens; D Tibboel; A de Klein; B Lee; D A Scott
Journal: Am J Hum Genet Date: 2007-04-04 Impact factor: 11.025

5. Identification of TCTE3 as a gene responsible for congenital diaphragmatic hernia using a high-resolution single-nucleotide polymorphism array.

Authors: Risa Teshiba; Kouji Masumoto; Genshiro Esumi; Kouji Nagata; Yoshiaki Kinoshita; Tatsuro Tajiri; Tomoaki Taguchi; Ken Yamamoto
Journal: Pediatr Surg Int Date: 2011-02 Impact factor: 1.827

5 in total