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Diaphragmatic hernia 2
- ... that condition. Congenital diaphragmatic defect Genetic Testing Registry: Diaphragmatic hernia 2 Genetic Testing Registry: Diaphragmatic hernia 3 Congenital diaphragmatic ...
- ... K, Devlieger H, Lauweryns JM. The syndrome of diaphragmatic hernia, abnormal face and distal limb anomalies (Fryns syndrome): report of two sibs with further delineation of this multiple congenital ...
- ... disomy (UPD). UPD occurs when a person receives two copies of a chromosome, or part of a ... hernia-exomphalos-corpus callosum agenesis Diaphragmatic hernia-exomphalos-hypertelorism ...
- ... cavity (the diaphragm), which is called a congenital diaphragmatic hernia. Meacham syndrome is typically fatal in infancy. Approximately ... WT1 gene most often cause diffuse glomerulosclerosis. WIT-2 WT1_HUMAN WT33 Tests of WT1 PubMed WT1 ...
- ... hernia), or a hole in the diaphragm (a diaphragmatic hernia) that allows the stomach and intestines to move ... they designated as Simpson-Golabi-Behmel syndrome type 2 (SGBS2). The signs and symptoms of this disorder ...
- ... of affected infants are born with a congenital diaphragmatic hernia, which is a hole in the muscle that ... i(12p). An isochromosome is a chromosome with two identical arms. Normal chromosomes have one long (q) ...
- ... cavity (the diaphragm), a condition called a congenital diaphragmatic hernia. Lethal multiple pterygium syndrome is typically fatal in ... subunit. Am J Hum Genet. 2006 Aug;79(2):303-12. doi: 10.1086/506257. Epub 2006 ...
- ... chest cavity (the diaphragm), which is called a diaphragmatic hernia, may occur in people with this disorder. Affected ... the X chromosome, which is one of the two sex chromosomes. In females (who have two X ...