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Items: 1 to 20 of 521

1.

Fryns syndrome: a lethal mesoectodermal birth defect with variable expression in a pair of monozygotic twins.

Pratap A, Agrawal A, Raja S, Khaniya S, Tiwari A, Kumar A.

Singapore Med J. 2007 Apr;48(4):e106-8.

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3.

Fryns syndrome without diaphragmatic hernia. Report on a new case and review of the literature.

Alessandri L, Brayer C, Attali T, Samperiz S, Tiran-Rajaofera I, Ramful D, Pilorget H.

Genet Couns. 2005;16(4):363-70. Review.

PMID:
16440878
4.

Discordant phenotype in monozygotic twins with Fryns syndrome.

Vargas JE, Cox GF, Korf BR.

Am J Med Genet. 2000 Sep 4;94(1):42-5.

PMID:
10982481
5.

Fryns syndrome: a lethal birth defect with variable phenotypic expressions in siblings.

Arora K, Thukral A, Das RR, Gupta N, Kabra M, Agarwal R.

Indian J Pediatr. 2014 Jun;81(6):614-6. doi: 10.1007/s12098-013-1011-1. Epub 2013 Apr 19.

PMID:
23604607
6.

Fryns syndrome: another example of non-lethal outcome with severe mental handicap.

Hanssen AM, Schrander-Stumpel CT, Thiry PA, Fryns JP.

Genet Couns. 1992;3(4):187-93.

PMID:
1472353
8.

Fryns syndrome: a rare familial cause of congenital diaphragmatic hernia.

Langer JC, Winthrop AL, Whelan D.

J Pediatr Surg. 1994 Sep;29(9):1266-7.

PMID:
7807364
9.

[Fryns syndrome: report of the first case in the national literature].

Rentería-Ibarra M, Frías-Márquez SG, Michel-Aceves RJ, Navarrete-Arellano M.

Bol Med Hosp Infant Mex. 1993 Sep;50(9):666-70. Spanish.

PMID:
8373549
10.

Fryns syndrome a presentation of two siblings with congenital diaphragmatic hernia.

Aboud MJ, Al-Shamsy MM.

Pediatr Surg Int. 2011 Jun;27(6):567-71. doi: 10.1007/s00383-010-2831-y.

PMID:
21259013
11.

Diaphragmatic defects, craniofacial dysmorphism, cleft palate and distal limb deformities. - a new lethal syndrome.

Goddeeris P, Fryns JP, van den Berghe H.

J Genet Hum. 1980 Mar;28(1):57-60.

PMID:
7400786
12.

Skeletal manifestations in Fryns syndrome.

Tsukahara M, Sase M, Tateishi H, Saito T, Kato H, Furukawa S.

Am J Med Genet. 1995 Jan 16;55(2):217-20. Review.

PMID:
7717421
13.

Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome.

Bamforth JS, Leonard CO, Chodirker BN, Chitayat D, Gritter HL, Evans JA, Keena B, Pantzar T, Friedman JM, Hall JG.

Am J Med Genet. 1989 Jan;32(1):93-9.

PMID:
2650550
15.

[Fryns syndrome--pre and postnatal diagnosis].

Dix U, Beudt U, Langenbeck U.

Z Geburtshilfe Perinatol. 1991 Nov-Dec;195(6):280-4. German.

PMID:
1776320
16.

Fryns syndrome: a surviving case with associated Hirschsprung's disease and hemidiaphragmatic agenesis.

Davis C, Samarakkody U.

J Paediatr Child Health. 2002 Jun;38(3):318-20.

PMID:
12047706
17.

Fryns syndrome: a predictable, lethal pattern of multiple congenital anomalies.

Samueloff A, Navot D, Birkenfeld A, Schenker JG.

Am J Obstet Gynecol. 1987 Jan;156(1):86-8.

PMID:
3799773
18.

Williams-Beuren syndrome in monozygotic twins with variable expression.

Pankau R, Gosch A, Simeoni E, Wessel A.

Am J Med Genet. 1993 Sep 15;47(4):475-7.

PMID:
8256808
19.

Monozygotic twins discordant for the Russell-Silver syndrome.

Samn M, Lewis K, Blumberg B.

Am J Med Genet. 1990 Dec;37(4):543-5.

PMID:
2260605
20.

Two fetuses with Fryns syndrome without diaphragmatic defects.

Wilgenbus KK, Engers R, Crombach G, Majewski F.

J Med Genet. 1994 Dec;31(12):962-4.

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