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4. Juberg-Hayward syndrome: report of a new patient with severe phenotype and novel clinical features. Hedera P; Innis JW Am J Med Genet A; 2003 Oct; 122A(3):257-60. PubMed ID: 12966528 [TBL] [Abstract][Full Text] [Related]
5. Juberg-Hayward syndrome is a cohesinopathy, caused by mutation in ESCO2. Kantaputra PN; Dejkhamron P; Intachai W; Ngamphiw C; Kawasaki K; Ohazama A; Krisanaprakornkit S; Olsen B; Tongsima S; Ketudat Cairns JR Eur J Orthod; 2021 Jan; 43(1):45-50. PubMed ID: 32255174 [TBL] [Abstract][Full Text] [Related]
6. A novel chromosomal aberration in a child with suspected Juberg-Hayward syndrome. Berger M; Rost I; Schmidt H Clin Dysmorphol; 2011 Apr; 20(2):121-126. PubMed ID: 21326092 [No Abstract] [Full Text] [Related]
7. A case of the orocraniodigital (Juberg-Hayward) syndrome. Nevin NC; Henry P; Thomas PT J Med Genet; 1981 Dec; 18(6):478-80. PubMed ID: 6278147 [TBL] [Abstract][Full Text] [Related]
8. Juberg-Hayward syndrome: report of a case with cleft palate, distally placed thumbs and vertebral anomalies. Silengo M; Tornetta L Clin Dysmorphol; 2000 Apr; 9(2):127-9. PubMed ID: 10826626 [TBL] [Abstract][Full Text] [Related]
9. Beemer-Langer syndrome with manifestations of an orofaciodigital syndrome. Lin AE; Doshi N; Flom L; Tenenholz B; Filkins KL Am J Med Genet; 1991 Jun; 39(3):247-51. PubMed ID: 1867273 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Syndrome of polydactyly, cleft lip, lingual hamartomas, renal hypoplasia, hearing loss, and psychomotor retardation: variant of the Mohr syndrome or a new syndrome? Mattei JF; Aymé S J Med Genet; 1983 Dec; 20(6):433-5. PubMed ID: 6686259 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. [25 years' history of Váradi-Papp syndrome (orofaciodigital syndrome VI]. Váradi V; Papp Z Orv Hetil; 2005 Sep; 146(39):2017-22. PubMed ID: 16265870 [TBL] [Abstract][Full Text] [Related]
14. New familial syndrome of unilateral upper eyelid coloboma, aberrant anterior hairline pattern, and anal anomalies in Manitoba Indians. Marles SL; Greenberg CR; Persaud TV; Shuckett EP; Chudley AE Am J Med Genet; 1992 Apr; 42(6):793-9. PubMed ID: 1554017 [TBL] [Abstract][Full Text] [Related]
15. Orofaciodigital syndrome type I in a girl with unilateral tibial pseudarthrosis. Orstavik KH; Tangsrud SE; Nordshus T; Finnanger AM; Hellum C; Gjessing E J Med Genet; 1992 Nov; 29(11):827-30. PubMed ID: 1453437 [TBL] [Abstract][Full Text] [Related]
16. [The differential diagnosis of Papillon-Lénge-Psaume-syndrome and Mohr's syndrome]. Fuhrmann W; Stahl A Humangenetik; 1970; 9(1):54-63. PubMed ID: 5488996 [No Abstract] [Full Text] [Related]
17. Prenatal diagnosis of a case probably with Oral-Facial-Digital Syndrome--Gabrielli type. Güven MA; Ceylaner G; Ceylaner S; Uzel M; Coskun A Genet Couns; 2009; 20(2):167-72. PubMed ID: 19650414 [TBL] [Abstract][Full Text] [Related]
18. Orofaciodigital syndrome I: a case report. Gunbay S; Zeytinoglu B; Ozkinay F; Ozkinay C; Oncag A J Clin Pediatr Dent; 1996; 20(4):329-32. PubMed ID: 9151628 [TBL] [Abstract][Full Text] [Related]
19. Oral-facial-digital syndrome type I: surgical approach and a case report. González MG; Castro MP; Nieto DV; Bouzán JC J Plast Reconstr Aesthet Surg; 2014 Mar; 67(3):396-8. PubMed ID: 23886557 [TBL] [Abstract][Full Text] [Related]