141 related articles for article (PubMed ID: 8205325)
21. Cerebellar hypoplasia, facial dysmorphism and internal abnormalities: a new recessive syndrome?
Seller MJ; Pal K; Moscoso G; Nicolaides K; Hyett JA
Clin Dysmorphol; 1998 Jan; 7(1):41-4. PubMed ID: 9546829
[TBL] [Abstract][Full Text] [Related]
22. Acrocallosal syndrome in fetus: focus on additional brain abnormalities.
Fernandez C; Soulier M; Coulibaly B; Liprandi A; Benoit B; Giuliano F; Sigaudy S; Figarella-Branger D; Fallet-Bianco C
Acta Neuropathol; 2008 Jan; 115(1):151-6. PubMed ID: 17593378
[TBL] [Abstract][Full Text] [Related]
23. [Femoral hypoplasia-unusual facies syndrome].
Ohashi H
Ryoikibetsu Shokogun Shirizu; 2001; (33):670-1. PubMed ID: 11462625
[No Abstract] [Full Text] [Related]
24. The femoral hypoplasia-unusual facies syndrome.
Burn J; Winter RM; Baraitser M; Hall CM; Fixsen J
J Med Genet; 1984 Oct; 21(5):331-40. PubMed ID: 6502648
[TBL] [Abstract][Full Text] [Related]
25. Molecular analysis of non-syndromic preaxial polydactyly: preaxial polydactyly type-IV and preaxial polydactyly type-I.
Fujioka H; Ariga T; Horiuchi K; Otsu M; Igawa H; Kawashima K; Yamamoto Y; Sugihara T; Sakiyama Y
Clin Genet; 2005 May; 67(5):429-33. PubMed ID: 15811011
[TBL] [Abstract][Full Text] [Related]
26. Preaxial polydactyly in the 4p- syndrome.
Schrander-Stumpel CT; Rijnvos WP; van der Blij-Philipsen M; Drogtrop A; Smeets D; Fryns JP
Genet Couns; 1998; 9(1):63-5. PubMed ID: 9555593
[No Abstract] [Full Text] [Related]
27. Prenatal diagnosis and tridimensional ultrasound features of bilateral femoral hypoplasia--unusual facies syndrome.
Figueroa C; Plasencia W; Eguiluz I; De Luis M; Barber MA; Valle L; García-Hernández JA
J Matern Fetal Neonatal Med; 2009 Oct; 22(10):936-9. PubMed ID: 19488946
[TBL] [Abstract][Full Text] [Related]
28. [Femoral hypoplasia and unusual facies. A syndrome of variable expressivity].
Selman E; Cantín A; Bancalari A
Rev Chil Pediatr; 1984; 55(2):100-3. PubMed ID: 6473848
[No Abstract] [Full Text] [Related]
29. Prenatal diagnosis of femoral facial syndrome: Three case reports and literature review.
Luisin M; Chevreau J; Klein C; Naepels P; Demeer B; Mathieu-Dramard M; Jedraszak G; Gondry-Jouet C; Gondry J; Dieux-Coeslier A; Morin G
Am J Med Genet A; 2017 Nov; 173(11):2923-2946. PubMed ID: 28948695
[TBL] [Abstract][Full Text] [Related]
30. Bilateral ulna hypoplasia, club feet, and mental retardation: a new mesomelic syndrome.
Kohn G; Malinger G; el Shawwa R; Scheinfeld A; Tepper R; Ornoy A; Lachman R; Rimoin DL
Am J Med Genet; 1995 Mar; 56(2):132-5. PubMed ID: 7625433
[TBL] [Abstract][Full Text] [Related]
31. Brief clinical report: femoral hypoplasia--unusual facies syndrome.
Hurst D; Johnson DF
Am J Med Genet; 1980; 5(3):255-8. PubMed ID: 7405957
[TBL] [Abstract][Full Text] [Related]
32. Prenatal diagnosis of femoral-facial syndrome: report of two cases.
Silvas E; Rypens F; Jovanovic M; Delezoide AL; Patey N
Birth Defects Res A Clin Mol Teratol; 2013 Dec; 97(12):770-3. PubMed ID: 24254654
[TBL] [Abstract][Full Text] [Related]
33. Case report: femoral hypoplasia - unusual facies syndrome.
Pitt DB; Findlay II; Cole WG; Rogers JG
Aust Paediatr J; 1982 Mar; 18(1):63-6. PubMed ID: 7103883
[No Abstract] [Full Text] [Related]
34. Femoral hypoplasia-unusual facies syndrome with renal agenesis and patent ductus arteriosus.
Aksoy HT; Eras Z; Simşek GK; Uraş N; Altug N; Dilmen U
Genet Couns; 2013; 24(3):351-5. PubMed ID: 24341153
[No Abstract] [Full Text] [Related]
35. The femoral hypoplasia-unusual facies syndrome: a genetic entity?
Lord J; Beighton P
Clin Genet; 1981 Oct; 20(4):267-75. PubMed ID: 7333019
[TBL] [Abstract][Full Text] [Related]
36. Dominant inheritance of femoral hypoplasia-unusual facies syndrome.
Lampert RP
Clin Genet; 1980 Apr; 17(4):255-8. PubMed ID: 7371218
[TBL] [Abstract][Full Text] [Related]
37. A 34-week-old male fetus with short rib polydactyly syndrome (SRPS) type I (Saldino-Noonan) with pancreatic cysts.
Balci S; Altinok G; Tekşen F; Eryilmaz M
Turk J Pediatr; 2003; 45(2):174-8. PubMed ID: 12921311
[TBL] [Abstract][Full Text] [Related]
38. [Femoral hypoplasia--unusual facies syndrome].
Trabelsi M; Monastiri K; Hammami A; Touzi C; Ben Hariz M; Gharbi HA; Bennaceur B
Ann Pediatr (Paris); 1989 Dec; 36(10):693-6. PubMed ID: 2624385
[TBL] [Abstract][Full Text] [Related]
39. Unknown syndrome: abnormal facies, hypothyroidism, postaxial polydactyly, and severe retardation: a third patient.
Cavalcanti DP
J Med Genet; 1989 Dec; 26(12):785-6. PubMed ID: 2614801
[TBL] [Abstract][Full Text] [Related]
40. Autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias.
Guttmacher AE
Am J Med Genet; 1993 Apr; 46(2):219-22. PubMed ID: 8484413
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
