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16 in total

1. At least nine cases of trisomy 11q23-->qter in one generation as a result of familial t(11;13) translocation.

Authors: D Smeets; C van Ravenswaaij; J de Pater; K Gerssen-Schoorl; J Van Hemel; G Janssen; A Smits
Journal: J Med Genet Date: 1997-01 Impact factor: 6.318

2. Radiology of postnatal skeletal development. III. The clavicle.

Authors: J A Ogden; G J Conlogue; M L Bronson
Journal: Skeletal Radiol Date: 1979 Impact factor: 2.199

Review 3. Cleidocranial dysplasia: clinical and molecular genetics.

Authors: S Mundlos
Journal: J Med Genet Date: 1999-03 Impact factor: 6.318

4. Congenital diaphragmatic hernia associated with duplication of 11q23-qter.

Authors: M Klaassens; D A Scott; M van Dooren; R Hochstenbach; H J Eussen; W W Cai; R J Galjaard; C Wouters; M Poot; J Laudy; B Lee; D Tibboel; A de Klein
Journal: Am J Med Genet A Date: 2006-07-15 Impact factor: 2.802

Review 5. Absence makes the search grow longer.

Authors: W B Dobyns
Journal: Am J Hum Genet Date: 1996-01 Impact factor: 11.025

6. The 11q -- syndrome.

Authors: J Frank; V M Riccardi
Journal: Hum Genet Date: 1977-02-11 Impact factor: 4.132

7. Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families.

Authors: A Schinzel; W Schmid; P Auf der Maur; H Moser; K H Degenhardt; M Geisler; A Grubisic
Journal: Hum Genet Date: 1981 Impact factor: 4.132

Duplication 11 (q21 to 23 leads to qter) syndrome.