UN LEPTODACTYLE PENTADACTYLE ECTRODACTYLE (AMPHIBIENS, ANOURES)DUBOIS A; FISCHER JL.1975; BULL. MENS. SOC. LINN. LYON; FR.; DA. 1975; VOL. 44; NO 4; PP. 111-114; ABS. ANGL.; BIBL. 15REF.Article

Isolated ectrodactyly caused by a heterozygous missense mutation in the transactivation domain of TP63ZENTENO, Juan Carlos; BERDON-ZAPATA, Valeria; KOFMAN-ALFARO, Susana et al.American journal of medical genetics. 2005, Vol 134A, Num 1, pp 74-76, issn 0148-7299, 3 p.Article

Syndrome FATCO―aplasie fibulaire, campomélie tibiale et oligosyndactylieVYSKOCIL, Vaclav; DORTOVA JIRI DORT, Eva; CHUDACEK, Zdenek et al.Revue du rhumatisme (Ed. française). 2011, Vol 78, Num 1, pp 96-97, issn 1169-8330, 2 p.Article

ISOLATED ECTRODACTYLY IN A NEWBORN WITH DOWN SYNDROMEKAVURT, S; CELIK, I. H; ADA, B. S et al.Genetic counseling. 2014, Vol 25, Num 2, pp 209-214, issn 1015-8146, 6 p.Article

Fibular aplasia with ectrodactyly : broadening the clinical spectrumGIERUSZCZAK-BIALEK, D; OLDAK, M; SKORKA, A et al.European journal of medical genetics. 2006, Vol 49, Num 1, pp 83-86, issn 1769-7212, 4 p.Article

Pierre Robin sequence in a patient with ectrodactyly-ectodermal dysplasia-clefting syndrome: a case report and review of the literatureJOHNSON, Steven E; TATUM, Sherard A; THOMSON, Laura L et al.International journal of pediatric otorhinolaryngology. 2002, Vol 66, Num 3, pp 309-313, issn 0165-5876, 5 p.Article

Prenatally Diagnosed Ectrodactyly at 16 Weeks' Gestation by 2-and 3-Dimensional Ultrasonography : A Case ReportBON SANG KOO; SU JIN BAEK; MI RYUNG KIM et al.Fetal diagnosis and therapy. 2008, Vol 24, Num 3, pp 161-164, issn 1015-3837, 4 p.Article

EEC syndrome sans clefting : Variable clinical presentations in a familyTHAKKAR, Sejal; MARFATIA, Yogesh.Indian Journal of Dermatology Venereology and Leprology. 2007, Vol 73, Num 1, pp 46-48, issn 0378-6323, 3 p.Article

Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformationEVERMAN, David B; MORGAN, Chad T; SCHRANDER-STUMPEL, Connie et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 13, pp 1375-1383, issn 1552-4825, 9 p.Article

A novel patient with cooks syndrome supports splitting from classic brachydactyly type BCASTORI, Marco; BRANCATI, Francesco; MINGARELLI, Rita et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 2, pp 195-199, issn 1552-4825, 5 p.Article

Tibial aplasia-hypoplasia and ectrodactyly in monozygotic twins with a discordant phenotypeDAYER, Romain; CERONI, Dimitri; BOTTANI, Armand et al.Journal of pediatric orthopedics. 2007, Vol 27, Num 3, pp 266-269, issn 0271-6798, 4 p.Article

Genotype-phenotype correlations in mapped split hand foot malformation (SHFM) patientsELLIOTT, Alison M; EVANS, Jane A.American journal of medical genetics. Part A. 2006, Vol 140, Num 13, pp 1419-1427, issn 1552-4825, 9 p.Article

DOMINANT ECTRODACTYLY AND POSSIBLE GERMINAL MOSAICISM = ECTRODACTYLIE DOMINANTE ET MOSAIQUE GERMINALE POSSIBLEDAVID TJ.1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 3; PP. 316-320; BIBL. 28REF.Serial Issue

Split-hand/split-foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the regionLYLE, Robert; RADHAKRISHNA, Uppala; GURRIERI, Fiorella et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 13, pp 1384-1395, issn 1552-4825, 12 p.Article

Microduplication of Xq24 and Hartsfield Syndrome With Holoprosencephaly, Ectrodactyly, and CleftingTAKENOUCHI, Toshiki; OKUNO, Hironobu; KOSAKI, Kenjiro et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 10, pp 2537-2541, issn 1552-4825, 5 p.Article

ECTRODACTYLY AND TETRALOGY OF FALLOT IN A FETUS WITH DEL(6)(q21q23)NOVIKOVA, I. V; LAZAREVICH, A. A; EGOROVA, T. M et al.Genetic counseling. 2014, Vol 25, Num 1, pp 19-27, issn 1015-8146, 9 p.Article

Clinical Variability in Acro-Cardio-Facial-SyndromeKARIMINEJAD, Ariana; BOZORGMEHR, Bita; MOHAMMAD ALL SEDIGHI GILANI et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 15, pp 1977-1979, issn 1552-4825, 3 p.Article

Dlx homeobox gene control of mammalian limb and craniofacial developmentKRAUS, Petra; LUFKIN, Thomas.American journal of medical genetics. Part A. 2006, Vol 140, Num 13, pp 1366-1374, issn 1552-4825, 9 p.Article

Bifurcation of the femur with tibial agenesis and additional anomaliesVAN DE KAMP, J. M; VAN DER SMAGT, J. J; BOS, C. F. A et al.American journal of medical genetics. 2005, Vol 138A, Num 1, pp 45-50, issn 0148-7299, 6 p.Article

Familial ectrodactyly―ectodermal dysplasia―clefting syndromeGÜN, Ismet; KIZILASLAN, Cem; ARAL ATALAY, Mehmet et al.International journal of gynaecology and obstetrics. 2012, Vol 119, Num 1, pp 86-87, issn 0020-7292, 2 p.Article

Holoprosencephaly and Ectrodactyly: Report of Three New Patients and Review of the LiteratureKEATON, Amelia A; SOLOMON, Benjamin D; VAN ESSEN, Anthonie J et al.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 1, pp 170-175, issn 1552-4868, 6 p.Article

Characterization of two ectrodactyly-associated translocation breakpoints separated by 2.5 Mb on chromosome 2q 14.1-q 14.2DAVID, Dezsö; MARQUES, Barbara; FERREIRA, Cristina et al.European journal of human genetics. 2009, Vol 17, Num 8, pp 1024-1033, issn 1018-4813, 10 p.Article

Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome Associated With p63 Mutation and an Uncommon PhenotypeRIBEIRO PARANAIBA, Livia Máris; MARTELLI-JUNIOR, Hercilio; TEIXEIRA DE MIRANDA, Roseli et al.The Cleft palate-craniofacial journal. 2010, Vol 47, Num 5, pp 544-547, issn 1055-6656, 4 p.Article

Ectrodactyly with fibular aplasia : A separate entity?MENKE, Leonie A; BIJLSMA, Emilia K; VAN ESSEN, Anthonie J et al.European journal of medical genetics. 2008, Vol 51, Num 5, pp 488-496, issn 1769-7212, 9 p.Article

Cadmium-induced postaxial forelimb ectrodactyly: association with altered sonic hedgehog signalingSCOTT, William J; SCHREINER, Claire M; GOETZ, John A et al.Reproductive toxicology (Elmsford, NY). 2005, Vol 19, Num 4, pp 479-485, issn 0890-6238, 7 p.Article