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1
Fryns syndrome: a lethal mesoectodermal birth defect with variable expression in a pair of monozygotic twins.
Singapore Med J. 2007 Apr;48(4):e106-8.
2
Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia.
Pediatrics. 1990 Apr;85(4):499-504.
3
Fryns syndrome: another example of non-lethal outcome with severe mental handicap.
Genet Couns. 1992;3(4):187-93.
4
The syndrome of diaphragmatic hernia, abnormal face and distal limb anomalies (Fryns syndrome): report of two sibs with further delineation of this multiple congenital anomaly (MCA) syndrome.
Am J Med Genet. 1988 Dec;31(4):805-14. doi: 10.1002/ajmg.1320310413.
5
Fryns syndrome without diaphragmatic hernia. Report on a new case and review of the literature.
Genet Couns. 2005;16(4):363-70.
6
[Fryns syndrome: report of the first case in the national literature].
Bol Med Hosp Infant Mex. 1993 Sep;50(9):666-70.
7
Diaphragmatic defects, craniofacial dysmorphism, cleft palate and distal limb deformities. - a new lethal syndrome.
J Genet Hum. 1980 Mar;28(1):57-60.
8
Skeletal manifestations in Fryns syndrome.
Am J Med Genet. 1995 Jan 16;55(2):217-20. doi: 10.1002/ajmg.1320550213.
9
Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome.
Am J Med Genet. 1989 Jan;32(1):93-9. doi: 10.1002/ajmg.1320320120.
10
Fryns syndrome: a lethal birth defect with variable phenotypic expressions in siblings.
Indian J Pediatr. 2014 Jun;81(6):614-6. doi: 10.1007/s12098-013-1011-1. Epub 2013 Apr 19.
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