220 related articles for article (PubMed ID: 8723090)
1. Jeune syndrome with tongue lobulation and preaxial polydactyly, and Jeune syndrome with situs inversus and asplenia: compound heterozygosity Jeune-Mohr and Jeune-Ivemark?
Majewski E; Oztürk B; Gillessen-Kaesbach G
Am J Med Genet; 1996 May; 63(1):74-9. PubMed ID: 8723090
[TBL] [Abstract][Full Text] [Related]
2. Orofaciodigital syndrome type IV (Mohr-Majewski syndrome) with severe expression expanding the known spectrum of anomalies.
Meinecke P; Hayek H
J Med Genet; 1990 Mar; 27(3):200-2. PubMed ID: 2325097
[TBL] [Abstract][Full Text] [Related]
3. Short rib-dysplasia group (with/without polydactyly): report of a patient suggesting the existence of a continuous spectrum.
Franceschini P; Guala A; Vardeu MP; Signorile F; Franceschini D; Bolgiani MP
Am J Med Genet; 1995 Nov; 59(3):359-64. PubMed ID: 8599362
[TBL] [Abstract][Full Text] [Related]
4. Naumoff short-rib polydactyly syndrome compounded with Mohr oral-facial-digital syndrome.
Young LW; Wilhelm LL; Zuppan CW; Clark R
Pediatr Radiol; 2001 Jan; 31(1):31-5. PubMed ID: 11200995
[TBL] [Abstract][Full Text] [Related]
5. Orofaciodigital syndrome type IV (Mohr-Majewski syndrome): report of a family with two affected siblings.
Kahl P; Heukamp LC; Buettner R; Friedrichs N; Roesing B; Knopfle G
Pediatr Dev Pathol; 2007; 10(3):239-43. PubMed ID: 17535085
[TBL] [Abstract][Full Text] [Related]
6. Oral-facial-digital syndrome type IV (Mohr-Majewski syndrome): a fetopathological study.
Moerman P; Fryns JP
Genet Couns; 1998; 9(1):39-43. PubMed ID: 9555586
[TBL] [Abstract][Full Text] [Related]
7. Oro-facial-digital syndrome II. Transitional type between the Mohr and the Majewski syndromes: report of two new cases.
Silengo MC; Bell GL; Biagioli M; Franceschini P
Clin Genet; 1987 May; 31(5):331-6. PubMed ID: 3608220
[TBL] [Abstract][Full Text] [Related]
8. Oral-facial-digital syndrome II. Transitional type between Mohr and Majewski syndrome: report of a new case with congenital stenosis of the trachea.
Steichen-Gersdorf E; Gassner I; Covi B; Fischer H
Clin Dysmorphol; 1994 Jul; 3(3):245-50. PubMed ID: 7981861
[TBL] [Abstract][Full Text] [Related]
9. Beemer-Langer type short rib-polydactyly syndrome: report of two cases.
Tsai FJ; Tsai CH; Wang TR
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1994; 35(4):331-4. PubMed ID: 8085456
[TBL] [Abstract][Full Text] [Related]
10. Lethal short rib-polydactyly syndromes: further evidence for their overlapping in a continuous spectrum.
Martínez-Frías ML; Bermejo E; Urioste M; Huertas H; Arroyo I
J Med Genet; 1993 Nov; 30(11):937-41. PubMed ID: 8301649
[TBL] [Abstract][Full Text] [Related]
11. Short rib polydactyly syndrome type 3 with absence of fibulae (Verma-Naumoff syndrome).
Kumru P; Aka N; Köse G; Vural ZT; Peker O; Kayserili H
Fetal Diagn Ther; 2005; 20(5):410-4. PubMed ID: 16113563
[TBL] [Abstract][Full Text] [Related]
12. Jeune asphyxiating thoracic dystrophy and short-rib polydactyly type III (Verma-Naumoff) are variants of the same disorder.
Ho NC; Francomano CA; van Allen M
Am J Med Genet; 2000 Feb; 90(4):310-4. PubMed ID: 10710229
[TBL] [Abstract][Full Text] [Related]
13. OFD II, OFD VI, and Joubert syndrome manifestations in 2 sibs.
Haug K; Khan S; Fuchs S; König R
Am J Med Genet; 2000 Mar; 91(2):135-7. PubMed ID: 10748413
[TBL] [Abstract][Full Text] [Related]
14. Short-rib polydactyly and Jeune syndromes are caused by mutations in WDR60.
McInerney-Leo AM; Schmidts M; Cortés CR; Leo PJ; Gener B; Courtney AD; Gardiner B; Harris JA; Lu Y; Marshall M; ; Scambler PJ; Beales PL; Brown MA; Zankl A; Mitchison HM; Duncan EL; Wicking C
Am J Hum Genet; 2013 Sep; 93(3):515-23. PubMed ID: 23910462
[TBL] [Abstract][Full Text] [Related]
15. Short rib syndrome--Beemer type in sibs.
Hennekam RC
Am J Med Genet; 1991 Aug; 40(2):230-3. PubMed ID: 1897578
[TBL] [Abstract][Full Text] [Related]
16. Oral-facial-digital syndrome with Y-shaped fourth metacarpals and endocardial cushion defect.
Hsieh YC; Hou JW
Am J Med Genet; 1999 Sep; 86(3):278-81. PubMed ID: 10482880
[TBL] [Abstract][Full Text] [Related]
17. Oral-facial-digital (OFD) syndrome with associated features: a new syndrome or genetic heterogeneity and variability?
Morán-Barroso V; Valdés Flores M; García-Cavazos R; Kofman-Alfaro S; Saavedra-Ontiveros D
Clin Dysmorphol; 1998 Jan; 7(1):55-7. PubMed ID: 9546832
[TBL] [Abstract][Full Text] [Related]
18. Absent pituitary gland and hypoplasia of the cerebellar vermis associated with partial ophthalmoplegia and postaxial polydactyly: a variant of orofaciodigital syndrome VI or a new syndrome?
Al-Gazali LI; Sztriha L; Punnose J; Shather W; Nork M
J Med Genet; 1999 Feb; 36(2):161-6. PubMed ID: 10051020
[TBL] [Abstract][Full Text] [Related]
19. Orofaciodigital syndrome type IV: report of a patient.
Nevin NC; Thomas PS
Am J Med Genet; 1989 Feb; 32(2):151-4. PubMed ID: 2929654
[TBL] [Abstract][Full Text] [Related]
20. Overlapping phenotypes in OFD type II and OFD type VI: report of two cases.
Panigrahi I; Das RR; Kulkarni KP; Marwaha RK
Clin Dysmorphol; 2013 Jul; 22(3):109-114. PubMed ID: 23459408
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
