12-year-old boy with a 4q35.2 microdeletion and involvement of MTNR1A, FAT1, and F11 genes.

Clinical dysmorphology

Volumn 21, Issue 2, 2012, Pages 93-96

  Youngs, Erin L ^a   Henkhaus, Rebecca S ^b   Hellings, Jessica A ^b   Butler, Merlin G ^b  

^a UNIVERSITY OF KANSAS SCHOOL OF MEDICINE   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 11; CADHERIN; FAT1 PROTEIN, HUMAN; MELATONIN 1 RECEPTOR;

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 4; CHROMOSOME DELETION; CHROMOSOME DISORDER; FACIES; GENETICS; HUMAN; MALE;

CADHERINS; CHILD; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 4; FACIES; FACTOR XI; HUMANS; MALE; RECEPTOR, MELATONIN, MT1;

EID: 85027922134     PISSN: None     EISSN: 14735717     Source Type: Journal    
DOI: 10.1097/mcd.0b013e32834e9216     Document Type: Article

References (0)