210 related articles for article (PubMed ID: 3608220)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. Abnormalities of the cerebellum in oro-facio-digital syndrome II (Mohr syndrome).
Annerén G; Gustavson KH; Jòzwiak S; Kjartansson S; Strömberg B
Clin Genet; 1990 Jul; 38(1):69-73. PubMed ID: 2387087
[TBL] [Abstract][Full Text] [Related]
7. Midline malformation syndromes.
Sharma AK; Phadke SR
Am J Med Genet; 1994 Apr; 50(3):304-5. PubMed ID: 8042679
[No Abstract] [Full Text] [Related]
8. 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]
9. Short rib (polydactyly) syndrome type IV: Beemer-Langer syndrome.
Sharma AK; Phadke SR; Agarwal SS
Am J Med Genet; 1993 May; 46(3):345-6. PubMed ID: 8488883
[No Abstract] [Full Text] [Related]
10. Further heterogeneity of the oral-facial-digital syndromes.
Townes PL; Wood BP; McDonald JV
Am J Dis Child; 1976 May; 130(5):548-54. PubMed ID: 179315
[TBL] [Abstract][Full Text] [Related]
11. Oro-facial-digital syndrome type II.
Kalyan M; Kanitkar S; John R; Gireesh G; Bhate A; Mithun M
J Assoc Physicians India; 2012 Oct; 60():50-2. PubMed ID: 23777026
[TBL] [Abstract][Full Text] [Related]
12. Hypothalamic hamartoma, cerebellar hypoplasia, facial dysmorphism and very atypical combination of polydactyly: is it a new variant of oro-facio-digital syndrome?
Okten A; Mungan L; Orhan F; Cakir M
Genet Couns; 2005; 16(1):101-5. PubMed ID: 15844787
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Perinatally lethal short rib-polydactyly syndromes. 1. Variability in known syndromes.
Sillence D; Kozlowski K; Bar-ziv J; Fuhrumann-Rieger A; Fuhrmann W; Pascu F
Pediatr Radiol; 1987; 17(6):474-80. PubMed ID: 3684360
[TBL] [Abstract][Full Text] [Related]
16. [Type-II orofaciodigital syndrome. Description of a case].
La Cava G; Gurrieri G; Mastroiacovo P
Pathologica; 1989; 81(1073):309-14. PubMed ID: 2641544
[TBL] [Abstract][Full Text] [Related]
17. Orofaciodigital syndrome Type IV (Mohr-Majewski): early prenatal diagnosis in siblings.
Rösing B; Kempe A; Berg C; Kahl P; Knöpfle G; Gembruch U; Geipel A
Ultrasound Obstet Gynecol; 2008 Apr; 31(4):457-60. PubMed ID: 18383484
[TBL] [Abstract][Full Text] [Related]
18. Oral-facial-digital syndrome: report on a transitional type between the Mohr and Váradi syndromes in a fetus.
Camera G; Marasini M; Pozzolo S; Camera A
Am J Med Genet; 1994 Nov; 53(2):196-8. PubMed ID: 7856648
[TBL] [Abstract][Full Text] [Related]
19. TCTN3 mutations cause Mohr-Majewski syndrome.
Thomas S; Legendre M; Saunier S; Bessières B; Alby C; Bonnière M; Toutain A; Loeuillet L; Szymanska K; Jossic F; Gaillard D; Yacoubi MT; Mougou-Zerelli S; David A; Barthez MA; Ville Y; Bole-Feysot C; Nitschke P; Lyonnet S; Munnich A; Johnson CA; Encha-Razavi F; Cormier-Daire V; Thauvin-Robinet C; Vekemans M; Attié-Bitach T
Am J Hum Genet; 2012 Aug; 91(2):372-8. PubMed ID: 22883145
[TBL] [Abstract][Full Text] [Related]
20. Orofaciodigital syndrome type II (Mohr syndrome): a case report.
Malekianzadeh B; Vosoughi F; Zargarbashi R
BMC Musculoskelet Disord; 2020 Nov; 21(1):793. PubMed ID: 33256699
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
