Prenatal diagnosis of an interstitial 12q chromosome deletion
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference10 articles.
1. Clinical application of multiplex quantitative fluorescent polymerase chain reaction (QF-PCR) for the rapid prenatal detection of common chromosome aneuploidies;Cirigliano;Mol. Hum. Reprod,2001
2. Prenatal ultrasound findings in affected and unaffected pregnancies that are scre-positive for trisomy 18: the California experience;Feuchtbaum;Prenatal Diagn.,2000
3. A new case of interstitial 12q deletion;Gallego;Int. Pediatr,2000
4. Prenatal diagnosis of de novo interstitial deletion of proximal 4q bu maternal serum screening for Down syndrome;Hsu;Prenatal Diagn.,1998
5. Multiple malformation syndrome including cleft lip and palate and cardiac abnormalities due to an interstitial deletion of chromosome 12q;Meinecke;J. Med. Genet,1985
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1. 12q21.2q22 deletion: A new patient;American Journal of Medical Genetics Part A;2015-04-06
2. Nasal speech and hypothyroidism are common hallmarks of 12q15 microdeletions;European Journal of Human Genetics;2011-04-20
3. A family with a 1.17 Mb deletion of 12q12: Refining genotype-phenotype correlation;American Journal of Medical Genetics Part A;2010-08-03
4. 12q12 deletion: A new patient contributing to genotype–phenotype correlation;American Journal of Medical Genetics Part A;2008
5. New case of interstitial deletion 12(q15-q21.2) in a girl with facial dysmorphism and mental retardation;American Journal of Medical Genetics Part A;2007
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