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Paper Details

Paternal or Maternal Uniparental Disomy of Chromosome 16 Resulting in Homozygosity of a Mutant Allele Causes Fanconi Anemia.
Hum Mutat
7
2016
FA, FANC genes, FANCA, FANCP, FANCP/SLX4 genes, Fanconi Anemia, Fanconi anemia, Mutant Allele, Paternal or Maternal Uniparental Disomy of Chromosome 16, SLX4, SNP arrays, UPD, bone marrow failure, cancer, child, chromosome 16, congenital abnormalities, inherited disorder, mutation-carrying chromosome 16, obligate mutant allele, patient, patients, recessive, short tandem repeat markers, uniparental disomy
Author NameAffiliation
Frank X DonovanNational Human Genome Research Institute
Danielle C KimbleNational Human Genome Research Institute
Francis P LachThe Rockefeller University
Ursula HarperNational Human Genome Research Institute
Ursula HarperNational Human Genome Research Institute
Aparna A KamatNational Human Genome Research Institute
Erica SanbornThe Rockefeller University
Elaine A OstranderNational Human Genome Research Institute
Elaine A OstranderNational Human Genome Research Institute
Arleen D AuerbachThe Rockefeller University
Agata SmogorzewskaThe Rockefeller University
Settara C ChandrasekharappaNational Human Genome Research Institute
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