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 journalLetter

8 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)385-387
Number of pages3
JournalAmerican journal of medical genetics
Volume140 A
Issue number4
DOIs
StatePublished - Feb 15 2006

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Multiple Abnormalities
Karyotyping
Chromosome Deletion
Chromosomes, Human, Pair 11
Fetal Growth Retardation
Metabolic Bone Diseases
Ventricular Heart Septal Defects
Hearing Loss
Phenotype

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

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 journalLetter

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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