195 related articles for article (PubMed ID: 15323276)
1. Fryns syndrome: a case associated with karyotype XO.
Dawani NM; Al Madhoob AR; Ali FA; Shabib F
Ann Saudi Med; 2004; 24(2):129-32. PubMed ID: 15323276
[No Abstract] [Full Text] [Related]
2. Fryns syndrome without diaphragmatic hernia, DOOR syndrome or Fryns-like syndrome? Report on patients from Indian Ocean islands.
Alessandri JL; Cuillier F; Malan V; Brayer C; Grondard M; Jacquemot-Dekkak L; Kieffer-Traversier M; Pierre F; Laurain C; Samperiz S; Tiran-Rajaofera I; Ramful D
Am J Med Genet A; 2014 Mar; 164A(3):648-54. PubMed ID: 24357154
[TBL] [Abstract][Full Text] [Related]
3. Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): a possible locus for Fryns syndrome.
Kantarci S; Casavant D; Prada C; Russell M; Byrne J; Haug LW; Jennings R; Manning S; Boyd TK; Fryns JP; Holmes LB; Donahoe PK; Lee C; Kimonis V; Pober BR
Am J Med Genet A; 2006 Jan; 140(1):17-23. PubMed ID: 16333846
[TBL] [Abstract][Full Text] [Related]
4. [Fryns syndrome. Report on 3 new cases].
Alessandri JL; Attali T; Brayer C; Dupuy L; Pilorget H; Ramful D; Samperiz S; Tiran-Rajaofera I; Robin S
Arch Pediatr; 2007 Jul; 14(7):903-7. PubMed ID: 17442547
[TBL] [Abstract][Full Text] [Related]
5. Craniorachischisis Totalis with Congenital Diaphragmatic Hernia-A Rare Presentation of Fryns Syndrome.
Singh A; Pilli GS; Bannur H
Fetal Pediatr Pathol; 2016; 35(3):192-8. PubMed ID: 27064748
[TBL] [Abstract][Full Text] [Related]
6. Skeletal manifestations in Fryns syndrome.
Tsukahara M; Sase M; Tateishi H; Saito T; Kato H; Furukawa S
Am J Med Genet; 1995 Jan; 55(2):217-20. PubMed ID: 7717421
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 21259013
[TBL] [Abstract][Full Text] [Related]
8. A case of Fryns syndrome without diaphragmatic hernia and review of the literature.
Vasudevan PC; Stewart H
Clin Dysmorphol; 2004 Jul; 13(3):179-182. PubMed ID: 15194956
[TBL] [Abstract][Full Text] [Related]
9. 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. PubMed ID: 17384863
[TBL] [Abstract][Full Text] [Related]
10. [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. PubMed ID: 8373549
[TBL] [Abstract][Full Text] [Related]
11. Cystic hygroma and congenital diaphragmatic hernia: early prenatal sonographic evaluation of Fryns' syndrome.
Bulas DI; Saal HM; Allen JF; Kapur S; Nies BM; Newman K
Prenat Diagn; 1992 Nov; 12(11):867-75. PubMed ID: 1494539
[TBL] [Abstract][Full Text] [Related]
12. Fryns syndrome.
Jog SM; Patole SK; Whitehall JS
J Postgrad Med; 2002; 48(2):129-30. PubMed ID: 12215698
[No Abstract] [Full Text] [Related]
13. Pulmonary agenesis, microphthalmia, and diaphragmatic defect (PMD): new syndrome or association?
Berkenstadt M; Lev D; Achiron R; Rosner M; Barkai G
Am J Med Genet; 1999 Sep; 86(1):6-8. PubMed ID: 10440821
[TBL] [Abstract][Full Text] [Related]
14. Diaphragmatic hernia and Fryns syndrome phenotype in partial trisomy 22.
de Beaufort C; Schneider F; Chafai R; Colette JM; Delneste D; Pierquin G
Genet Couns; 2000; 11(2):181-2. PubMed ID: 10893671
[No Abstract] [Full Text] [Related]
15. Craniocervical junction malformation in a child with Oromandibular-limb hypogenesis-Möbius syndrome.
Al Kaissi A; Grill F; Safi H; Ben Ghachem M; Ben Chehida F; Klaushofer K
Orphanet J Rare Dis; 2007 Jan; 2():2. PubMed ID: 17210070
[TBL] [Abstract][Full Text] [Related]
16. Fryns syndrome: a review of the phenotype and diagnostic guidelines.
Slavotinek AM
Am J Med Genet A; 2004 Feb; 124A(4):427-33. PubMed ID: 14735597
[TBL] [Abstract][Full Text] [Related]
17. 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. PubMed ID: 23604607
[TBL] [Abstract][Full Text] [Related]
18. Fryns syndrome phenotype and trisomy 22.
Ladonne JM; Gaillard D; Carré-Pigeon F; Gabriel R
Am J Med Genet; 1996 Jan; 61(1):68-70. PubMed ID: 8741922
[TBL] [Abstract][Full Text] [Related]
19. 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. PubMed ID: 16440878
[TBL] [Abstract][Full Text] [Related]
20. Fryns syndrome: neurologic findings in a survivor.
Riela AR; Thomas IT; Gonzalez AR; Ifft RD
J Child Neurol; 1995 Mar; 10(2):110-3. PubMed ID: 7782599
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
