Interstitial and terminal deletions of the long arm of chromosome 4: Further delineation of phenotypes
Lin A.G., Garver K.L., Giggans K.L., Clemens M., Wayne S.L., Steele M.W., et al. Interstitial and terminal deletions of the long arm of chromosome 4: Further delineation of phenotypes. Ann J Med Genet 31 (1988) 533-548
Terminal deletion of the long arm of chromosome 4 in a mother and two sons
Descartes M., Keppler-Noreuil K., Knops J., Longshore J.W., Finlay W.H., Carroll A.S., et al. Terminal deletion of the long arm of chromosome 4 in a mother and two sons. J Clin Genet 50 (1996) 538-540
The tale of a nail sign in chromosome 4q34 deletion syndrome
Vogt J., Ryan E., Tischkowotz M.D., Reardon W., and Brueton L.A. The tale of a nail sign in chromosome 4q34 deletion syndrome. Clin Dysmorphol 15 (2006) 127-132
Terminal deletion of the long arm of chromosome 4: Report of a case of 46, XY, del (4) (q31) and review of 4q syndrome
Yu W., Chen H., Baucum R.W., and Hand A.M. Terminal deletion of the long arm of chromosome 4: Report of a case of 46, XY, del (4) (q31) and review of 4q syndrome. Ann Genet 24 (1981) 158-161
A new case of an interstitial deletion of (4) (q25q27) characterized by molecular cytogenetic techniques and review of the literature
Becker S.A., Popp S., Rager K., and Jauch A. A new case of an interstitial deletion of (4) (q25q27) characterized by molecular cytogenetic techniques and review of the literature. Eur J Paediatr 162 (2003) 267-270
Syndrome of terminal deletion of the long arm of chromosome 4: Apropos of a personal case with a review of the literature
Frappaz D., Bourgeois J., Berthier J.C., Laurent C., and Bethenod M. Syndrome of terminal deletion of the long arm of chromosome 4: Apropos of a personal case with a review of the literature. Pediatrie 38 (1983) 261-270
Interstitial deletions 4q21.1q25 and 4q25q27: Phenotypic variability and relation to Reiger anomaly
Kulharya A.S., Maberry M., Kukolich M.K., Day D.W., Schneider W.R., and Wilson G.N. Interstitial deletions 4q21.1q25 and 4q25q27: Phenotypic variability and relation to Reiger anomaly. Am J Med Genet 16 (1995) 165-170
