83 related articles for article (PubMed ID: 10319201)
1. Juberg-Hayward syndrome: a new case report and clinical delineation of the syndrome.
Kantaputra PN; Mongkolchaisup S
Clin Dysmorphol; 1999 Apr; 8(2):123-7. PubMed ID: 10319201
[TBL] [Abstract][Full Text] [Related]
2. Lujan-Fryns syndrome (X-linked mental retardation with marfanoid habitus): report of three cases and review.
Lacombe D; Bonneau D; Verloes A; Couet D; Koulischer L; Battin J
Genet Couns; 1993; 4(3):193-8. PubMed ID: 8267926
[TBL] [Abstract][Full Text] [Related]
3. [A complex symphalangia syndrome with brachydactyly, humeroradial synostosis and other multiple joint dysplasias].
Schumacher KA; Wolf M; Friedrich JM
Rontgenblatter; 1988 May; 41(5):211-4. PubMed ID: 3393818
[TBL] [Abstract][Full Text] [Related]
4. Brachydactyly, mesomelia, mental retardation, aortic dilatation, mitral valve prolapse, and characteristic face.
Stratton RF; Garcia PR; Young RS; Jorgenson RJ
Am J Med Genet; 1993 Apr; 46(2):138-41. PubMed ID: 8484398
[TBL] [Abstract][Full Text] [Related]
5. Agenesis of the corpus callosum, camptodactyly and obesity.
Verloes A; Lesenfants S
Clin Dysmorphol; 2000 Apr; 9(2):107-9. PubMed ID: 10826621
[TBL] [Abstract][Full Text] [Related]
6. Spondylocarpotarsal synostosis with epiphyseal dysplasia.
Honeywell C; Langer L; Allanson J
Am J Med Genet; 2002 May; 109(4):318-22. PubMed ID: 11992487
[TBL] [Abstract][Full Text] [Related]
7. Juberg-Hayward syndrome and Roberts syndrome are allelic, caused by mutations in ESCO2.
Kantaputra PN; Dejkhamron P; Tongsima S; Ngamphiw C; Intachai W; Ngiwsara L; Sawangareetrakul P; Svasti J; Olsen B; Cairns JRK; Bumroongkit K
Arch Oral Biol; 2020 Nov; 119():104918. PubMed ID: 32977150
[TBL] [Abstract][Full Text] [Related]
8. Further report of a patient with humeroradioulnar synostosis and hydronephrosis.
Boy R; Horovitz D; Vargas FR; Barbosa Neto JG; Llerena Júnior JC; Almeida JC
J Med Genet; 1995 Jan; 32(1):78-9. PubMed ID: 7897637
[No Abstract] [Full Text] [Related]
9. Pseudoaminopterin syndrome.
Verloes A; Bricteux G; Koulischer L
Am J Med Genet; 1993 Jun; 46(4):394-7. PubMed ID: 8357010
[TBL] [Abstract][Full Text] [Related]
10. The KBG syndrome: an additional sporadic case.
Mathieu M; Helou M; Morin G; Dolhem P; Devauchelle B; Piussan C
Genet Couns; 2000; 11(1):33-5. PubMed ID: 10756425
[TBL] [Abstract][Full Text] [Related]
11. Congenital anomalies of the upper extremity.
Dobyns JH; Doyle JR; Von Gillern TL; Cowen NJ
Hand Clin; 1989 Aug; 5(3):321-42; discussion 339-340. PubMed ID: 2549079
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Skeletal dysplasia syndrome with progeroid appearance, characteristic facial and limb anomalies, multiple synostoses, and distinct skeletal changes: a variant example of the Lenz-Majewski syndrome.
Chrzanowska KH; Fryns JP; Krajewska-Walasek M; Van den Berghe H; Wisniewski L
Am J Med Genet; 1989 Apr; 32(4):470-4. PubMed ID: 2773987
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Unilateral longitudinal radial ray deficiency of the hand and metacarpal 4-5 synostosis.
De Smet L; Keymolen K; Fryns JP
Genet Couns; 1999; 10(4):369-72. PubMed ID: 10631924
[TBL] [Abstract][Full Text] [Related]
16. Mild case of Curry-Jones syndrome.
Thomas ER; Wakeling EL; Goodman FR; Dickinson JC; Hall CM; Brady AF
Clin Dysmorphol; 2006 Apr; 15(2):115-7. PubMed ID: 16531740
[TBL] [Abstract][Full Text] [Related]
17. Possible third case of Lin-Gettig syndrome.
Hedera P; Innis JW
Am J Med Genet; 2002 Jul; 110(4):380-3. PubMed ID: 12116213
[TBL] [Abstract][Full Text] [Related]
18. Report of a new syndrome: focus on differential diagnosis and review of Ellis-van Creveld, Curry-Hall, acrofacial dysostosis, and orofacial digital syndromes.
Ghosh S; Setty S; Sivakumar A; Pai KM
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2007 May; 103(5):670-6. PubMed ID: 17466885
[TBL] [Abstract][Full Text] [Related]
19. Additional case of Keipert syndrome and review of the literature.
Cappon SM; Khalifa MM
Med Sci Monit; 2000; 6(4):776-8. PubMed ID: 11208408
[TBL] [Abstract][Full Text] [Related]
20. [A case of Keutel syndrome in child (review the literature)].
Xu L; Xia Z; Liu X; Huang S
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Sep; 26(18):793-4. PubMed ID: 23259292
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]