Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial deletion of 7q (7q22.1→q31.1)
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference34 articles.
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4. Mutation screening and association analysis of six candidate genes for autism on chromosome 7q;Bonora;Eur. J. Hum. Genet.,2005
5. Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly;Chen;Taiwan. J. Obstet. Gynecol.,2011
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1. Clinical, cytogenetic, and molecular findings in a fetus with ultrasonic multiple malformations, 4q duplication, and 7q deletion;Medicine;2018-11
2. Array-comparative genomic hybridization analysis in patients with Müllerian fusion anomalies;Clinical Genetics;2018-02-05
3. Germline large genomic alterations on 7q in patients with multiple primary cancers;Scientific Reports;2017-01-31
4. Interstitial deletion of 7q22.1q31.1 in a boy with structural brain abnormality, cardiac defect, developmental delay, and dysmorphic features;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2016-04-20
5. A Novel 23.1 Mb Interstitial Deletion Involving 7q22.3q32.1 in a Girl with Short Stature, Motor Delay, and Craniofacial Dysmorphism;Cytogenetic and Genome Research;2015
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