Terminal deletion of 6q and Fryns syndrome : A microdeletion/syndrome Pair ?KRASSIKOFF, N; SEKHON, G. S.American journal of medical genetics. 1990, Vol 36, Num 3, pp 363-364, issn 0148-7299, 2 p.Article

FRYNS SYNDROME WITH VERTEBRAL DEFECTS: A NOVEL ASSOCIATION IN A MEXICAN INFANTSALINAS-TORRES, V. M; RIVERA, H.Genetic counseling. 2014, Vol 25, Num 1, pp 29-33, issn 1015-8146, 5 p.Article

Fryns syndrome in children with Congenital Diaphragmatic HerniaJournal of pediatric surgery. 2002, Vol 37, Num 12, pp 1685-1687, issn 0022-3468, 3 p.Article

Skeletal manifestations in Fryns syndromeTSUKAHARA, M; SASE, M; TATEISHI, H et al.American journal of medical genetics. 1995, Vol 55, Num 2, pp 217-220, issn 0148-7299Article

X-linked mental retardation with marfanoid habitus : a changing phenotype with age?FRYNS, J. P; VAN DEN BERGHE, H.Genetic counseling. 1991, Vol 2, Num 4, pp 241-244, issn 1015-8146Article

Lujans-Fryns syndrome in the differential diagnosis of schizophreniaDE HERT, M; STEEMANS, D; THEYS, P et al.American journal of medical genetics. 1996, Vol 67, Num 2, pp 212-214, issn 0148-7299Article

A 6-year-old child with Fryns syndrome: Further delineation of the natural history of the condition in survivorsDENTICI, Maria Lisa; BRANCATI, Francesco; MINGARELLI, Rita et al.European journal of medical genetics. 2009, Vol 52, Num 6, pp 421-425, issn 1769-7212, 5 p.Article

Fryns syndrome and erupted teeth in a 24-weeks-old fetusMANOUVRIER-HANU, S; DEVISME, L; VAAST, P et al.Genetic counseling. 1996, Vol 7, Num 2, pp 131-134, issn 1015-8146Conference Paper

Terminal deletion of chromosome 5p in a patient with phenotypical features of Lujan-Fryns syndromeSTATHOPULU, E; OGILVIE, C. Mackie; FLINTER, F. A et al.American journal of medical genetics. 2003, Vol 119A, Num 3, pp 363-366, issn 0148-7299, 4 p.Article

Fryns syndrome phenotype and trisomy 22LADONNE, J.-M; GAILLARD, D; CARRE-PIGEON, F et al.American journal of medical genetics. 1996, Vol 61, Num 1, pp 68-70, issn 0148-7299Article

Fryns syndrome survivors and neurologic outcomeVAN HOVE, J. L. K; SPIRIDIGLIOZZI, G. A; HEINZ, R et al.American journal of medical genetics. 1995, Vol 59, Num 3, pp 334-340, issn 0148-7299Article

Fryns syndrome: a variable MCA syndrome with diaphragmatic defects, coarse face, and distal limb hypoplasiaFRYNS, J. P.Journal of medical genetics. 1987, Vol 24, Num 5, pp 271-274, issn 0022-2593Article

Single gene disorders associated with congenital diaphragmatic herniaSLAVOTINEK, Anne M.American journal of medical genetics. Part C, Seminars in medical genetics. 2007, Vol 145, Num 2, pp 172-183, issn 1552-4868, 12 p.Article

Lujan-Fryns syndrome (X-linked mental retardation with marfanoid habitus): report of three cases and reviewLACOMBE, D; BONNEAU, D; VERLOES, A et al.Genetic counseling. 1993, Vol 4, Num 3, pp 193-198, issn 1015-8146Article

Un nouveau syndrome polymalformatif et subléthal associant hernie diaphragmatique, hypoplasie digitale distale et anomalies craniofaciales le «syndrome de Fryns» = The syndrome of diaphragmatic hernia, distal limb hypoplasia and coarse face C «Fryns Syndrome»FRYNS, J. P; MOERMAN, P; VAN DEN BEGHE, H et al.Journal de génétique humaine. 1989, Vol 37, Num 3, pp 203-205, issn 0021-7743Conference Paper

X-linked mental retardation with marfanoid habitus : first report of four Italian patientsLALATTA, F; LIVINI, E; SELICORNI, A et al.American journal of medical genetics. 1991, Vol 38, Num 2-3, pp 228-232, issn 0148-7299Article

Cleft-palate lateral synechia syndrome: Insight into the phenotypic spectrum of Fryns syndrome?JAEGER, April; KAPUR, Raj; WHELAN, Michael et al.Birth defects research. Clinical and molecular teratology. 2003, Vol 67, Num 6, pp 460-466, issn 1542-0752, 7 p.Article

Síndrome de Fryns: informe del primer caso en la literatura nacional = The Fryns' syndrome. Report of the first case in the Mexican literatureRENTERíA-IBARRA, M; FRÍAS-MÁRQUEZ, S. G; MICHEL-ACEVES, R. J et al.Boletín Médico del Hospital Infantil de México (Ed. española). 1993, Vol 50, Num 9, pp 666-670, issn 0539-6115Article

Eye abnormalities in Fryns syndromePIERSON, Diane M; TABOADA, Eugenio; BUTLER, Merlin G et al.American journal of medical genetics. 2004, Vol 125A, Num 3, pp 273-277, issn 0148-7299, 5 p.Article

Congenital Diaphragmatic Hernia and Microtia in a Newborn With Mycophenolate Mofetil (MMF) Exposure: Phenocopy for Fryns Syndrome or Broad Spectrum of Teratogenic Effects?PARISI, Melissa A; ZAYED, Hatem; SLAVOTINEK, Anne M et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 6, pp 1237-1240, issn 1552-4825, 4 p.Article

Pallister-Killian and Fryns Syndromes : nosologyMCPHERSON, E. W; KETTERER, D. M; SALSBUREY, D. J et al.American journal of medical genetics. 1993, Vol 47, Num 2, pp 241-245, issn 0148-7299Article

Anophthalmia-microphthalmia-oblique clefting syndrome: Confirmation of the Fryns anophthalmia syndromeWARBURG, M; JENSEN, H; PRAUSE, J. U et al.American journal of medical genetics. 1997, Vol 73, Num 1, pp 36-40, issn 0148-7299Article

Fryns syndrome in a girl born to consanguineous parentsSCHWYZER, U; BRINER, J; SCHINZEL, A et al.Acta paediatrica scandinavica. 1987, Vol 76, Num 1, pp 167-171, issn 0001-656XArticle

Fryns syndrome : another example of non-lethal outcome with severe mental handicapHANSSEN, A. M. N; SCHRANDER-STUMPEL, C. T. R. M; THIRY, P. A. E et al.Genetic counseling. 1992, Vol 3, Num 4, pp 187-193, issn 1015-8146Article

Apparent Fryns syndrome in a boy with a tandem duplication of 1q24-31.2CLARK, R. D; FENNER-GONZALES, M.American journal of medical genetics. 1989, Vol 34, Num 3, pp 422-426, issn 0148-7299Article