Cited by

• Characterization of a complex rearrangement involving duplication and deletion of 9p in an infant with craniofacial dysmorphism and cardiac anomalies.

  Di Bartolo DL, El Naggar M, Owen R, Sahoo T, Gilbert F, Pulijaal VR, Mathew S. Di Bartolo DL, et al. Mol Cytogenet. 2012 Jul 9;5(1):31. doi: 10.1186/1755-8166-5-31. Mol Cytogenet. 2012. PMID: 22768875 Free PMC article.
• Mental retardation and congenital malformations associated with a ring chromosome 9.

  Nakajima S, Yanagisawa M, Kamoshita S, Nakagome Y. Nakajima S, et al. Hum Genet. 1976 Jun 29;32(3):289-93. doi: 10.1007/BF00295818. Hum Genet. 1976. PMID: 939548
• A girl with karyotype 46,XX,del(7)(qter-p 15:).

  Friedrich U, Lyngbye T, Oster J. Friedrich U, et al. Humangenetik. 1975;26(2):161-5. doi: 10.1007/BF00278448. Humangenetik. 1975. PMID: 1112608
• Idiopathic central precocious puberty associated with 11 mb de novo distal deletion of the chromosome 9 short arm.

  Cisternino M, Della Mina E, Losa L, Madè A, Rossetti G, Bassi LA, Pieri G, Bayindir B, Messa J, Zuffardi O, Ciccone R. Cisternino M, et al. Case Rep Genet. 2013;2013:978087. doi: 10.1155/2013/978087. Epub 2013 Jul 31. Case Rep Genet. 2013. PMID: 23984122 Free PMC article.
• EARLY-ONSET GONADOBLASTOMA IN A 13-MONTH-OLD INFANT WITH 46,XY COMPLETE GONADAL DYSGENESIS IDENTIFIED WITH PRENATAL TESTING: A CASE OF CHROMOSOME 9p DELETION.

  Fredette ME, Cusmano K, Phornphutkul C, Schwab J, Caldamone A, Topor LS. Fredette ME, et al. AACE Clin Case Rep. 2019 Aug 14;5(6):e380-e383. doi: 10.4158/ACCR-2019-0285. eCollection 2019 Nov-Dec. AACE Clin Case Rep. 2019. PMID: 31967076 Free PMC article.