Novel clinical features in a child with partial deletion of chromosome 11 [del(11)(q24.2)]: Further evidence for phenotypic heterogeneity [1]

Philip F. Giampietro; Deepti Babu; Carrie A. Zabel; Teresa Silberman; Ivan Zador; David DeBauche; J. Britt Ravnan; Bhavana J. Dave

doi:10.1002/ajmg.a.31067

Novel clinical features in a child with partial deletion of chromosome 11 [del(11)(q24.2)]: Further evidence for phenotypic heterogeneity [1]

Philip F. Giampietro, Deepti Babu, Carrie A. Zabel, Teresa Silberman, Ivan Zador, David DeBauche, J. Britt Ravnan, Bhavana J. Dave

Research output: Contribution to journal › Letter

8 Scopus citations

Original language	English (US)
Pages (from-to)	385-387
Number of pages	3
Journal	American Journal of Medical Genetics
Volume	140 A
Issue number	4
DOIs	https://doi.org/10.1002/ajmg.a.31067
State	Published - Feb 15 2006

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1002/ajmg.a.31067

Cite this

Giampietro, P. F., Babu, D., Zabel, C. A., Silberman, T., Zador, I., DeBauche, D., Ravnan, J. B., & Dave, B. J. (2006). Novel clinical features in a child with partial deletion of chromosome 11 [del(11)(q24.2)]: Further evidence for phenotypic heterogeneity [1]. American Journal of Medical Genetics, 140 A(4), 385-387. https://doi.org/10.1002/ajmg.a.31067

Novel clinical features in a child with partial deletion of chromosome 11 [del(11)(q24.2)] : Further evidence for phenotypic heterogeneity [1]. / Giampietro, Philip F.; Babu, Deepti; Zabel, Carrie A.; Silberman, Teresa; Zador, Ivan; DeBauche, David; Ravnan, J. Britt; Dave, Bhavana J.

In: American Journal of Medical Genetics, Vol. 140 A, No. 4, 15.02.2006, p. 385-387.

Research output: Contribution to journal › Letter

Giampietro, Philip F. ; Babu, Deepti ; Zabel, Carrie A. ; Silberman, Teresa ; Zador, Ivan ; DeBauche, David ; Ravnan, J. Britt ; Dave, Bhavana J. / Novel clinical features in a child with partial deletion of chromosome 11 [del(11)(q24.2)] : Further evidence for phenotypic heterogeneity [1]. In: American Journal of Medical Genetics. 2006 ; Vol. 140 A, No. 4. pp. 385-387.

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