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 › peer-review

10 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

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@article{69bf58ff7f8c49ee962d158e9f8a2646,

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

author = "Giampietro, {Philip F.} and Deepti Babu and Zabel, {Carrie A.} and Teresa Silberman and Ivan Zador and David DeBauche and Ravnan, {J. Britt} and Dave, {Bhavana J.}",

year = "2006",

month = feb,

day = "15",

doi = "10.1002/ajmg.a.31067",

language = "English (US)",

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journal = "American Journal of Medical Genetics",

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T1 - Novel clinical features in a child with partial deletion of chromosome 11 [del(11)(q24.2)]

T2 - Further evidence for phenotypic heterogeneity [1]

AU - Giampietro, Philip F.

AU - Babu, Deepti

AU - Zabel, Carrie A.

AU - Silberman, Teresa

AU - Zador, Ivan

AU - DeBauche, David

AU - Ravnan, J. Britt

AU - Dave, Bhavana J.

PY - 2006/2/15

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DO - 10.1002/ajmg.a.31067

M3 - Letter

C2 - 16411193

AN - SCOPUS:32444448774

SN - 1552-4825

VL - 140 A

SP - 385

EP - 387

JO - American Journal of Medical Genetics

JF - American Journal of Medical Genetics

IS - 4

ER -

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

ASJC Scopus subject areas

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