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Article

Interstitial deletion of 11q in a mother and fetus: implications of directly transmitted chromosomal imbalances for prenatal genetic counseling

26 Feb 2009

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Share to Chromosomal and Genetic Variations
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 19177486
DOI: 10.1002/pd.2209

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Interstitial deletion of 11q in a mother and fetus: implications of directly transmitted chromosomal imbalances for prenatal genetic counselingPMID 19177486Read ↗

Prenatal and postnatal findings in a 10.6 Mb interstitial deletion at 10p11.22-p12.31.Semantic proximity Read ↗

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Deletion and duplication of 11p13-11p14: reciprocal aberrations derived from a paternal insertion.Semantic proximity Read ↗

Prenatal Diagnosis of Combined Maternal 4q Interstitial Deletion and Paternal 15q Microduplication.Semantic proximity Read ↗

Genome-wide noninvasive prenatal screening for carriers of balanced reciprocal translocationsSemantic proximity Read ↗

Maternal transmission of interstitial 8p23.1 deletion detected during prenatal diagnosis.Semantic proximity Read ↗

Genetic etiology and phenotypic characteristics of fetuses with 11q deletion (11q23.3-q25) syndromeSemantic proximity Read ↗

Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.Semantic proximity Read ↗

Duplications of chromosome 11p15 of maternal origin result in a phenotype that includes growth retardation.Semantic proximity Read ↗

Interstitial deletion of chromosome 11 (q22.3-q23.2) in a boy with mild developmental delay.Semantic proximity Read ↗

Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistrySemantic proximity Read ↗

De novo interstitial deletion in the long arm of chromosome 11: a case report.Semantic proximity Read ↗

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