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Medline ® Abstract for Reference 79

of 'Clinical manifestations and diagnosis of Fanconi anemia'

79
TI
X-linked recessive VACTERL-H due to a mutation in FANCB in a preterm boy.
AU
Mikat B, Roll C, Schindler D, Gembruch U, Klempert I, Buiting K, Bramswig NC, Wieczorek D
SO
Clin Dysmorphol. 2016 Apr;25(2):73-6.
 
AD
aInstitute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Duisburg and Essen bDepartment of Neonatology, Vest Children's Hospital Datteln, University Witten/Herdecke, Datteln cInstitute of Human Genetics, Biozentrum, University of Würzburg, Würzburg dDepartment of Obstetrics and Prenatal Medicine, University Bonn Medical School, Bonn eInstitute of Pathology, Charite - Universitaetsmedizin Berlin, Berlin, Germany.
PMID