94 related articles for article (PubMed ID: 9018415)
1. Unusual type of brachydactyly associated with intraventricular septal defect and deafness: a new condition?
Camera G; Costa M
Clin Dysmorphol; 1997 Jan; 6(1):31-3. PubMed ID: 9018415
[TBL] [Abstract][Full Text] [Related]
2. Brachydactyly type B: case report and further evidence for clinical heterogeneity.
Slavotinek A; Clayton-Smith J
Clin Dysmorphol; 1999 Jul; 8(3):165-71. PubMed ID: 10457848
[TBL] [Abstract][Full Text] [Related]
3. DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): a new patient and delineation of neurologic variability among recessive cases.
Lin HJ; Kakkis ED; Eteson DJ; Lachman RS
Am J Med Genet; 1993 Sep; 47(4):534-9. PubMed ID: 8256819
[TBL] [Abstract][Full Text] [Related]
4. Brachydactyly type A-4 (Temtamy type) with short stature in a Japanese girl and her mother.
Ohzeki T; Hanaki K; Motozumi H; Ohtahara H; Shiraki K; Yoshioka K
Am J Med Genet; 1993 May; 46(3):260-2. PubMed ID: 8387724
[TBL] [Abstract][Full Text] [Related]
5. Brachydactyly type A1 with short humerus and associated skeletal features.
Lacombe D; Delrue MA; Rooryck C; Morice-Picard F; Arveiler B; Maugey-Laulom B; Mundlos S; Toutain A; Chateil JF
Am J Med Genet A; 2010 Dec; 152A(12):3016-21. PubMed ID: 21077205
[TBL] [Abstract][Full Text] [Related]
6. Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome.
Morava E; Czakó M; Kárteszi J; Cser B; Weissbecker K; Méhes K
Clin Dysmorphol; 2003 Jul; 12(3):161-5. PubMed ID: 14564152
[TBL] [Abstract][Full Text] [Related]
7. A boy with severe manifestations of type A1 brachydactyly.
Slavotinek A; Donnai D
Clin Dysmorphol; 1998 Jan; 7(1):21-7. PubMed ID: 9546826
[TBL] [Abstract][Full Text] [Related]
8. [DOOR (deafness, onychodystrophy, osteodystrophy, mental retardation) syndrome].
Szabó L; Kocsis K; Hollódy K; Soroncz M; Erwa W; Andits M
Orv Hetil; 2004 May; 145(22):1183-7. PubMed ID: 15279406
[TBL] [Abstract][Full Text] [Related]
9. Embryology of familial (non-syndromic) brachydactyly of the hand.
Al-Qattan MM
J Hand Surg Eur Vol; 2014 Nov; 39(9):926-33. PubMed ID: 24300509
[TBL] [Abstract][Full Text] [Related]
10. Previously undescribed syndrome of craniofacial, hand anomalies, and sensorineural deafness.
Sommer A; Young-Wee T; Frye T
Am J Med Genet; 1983 May; 15(1):71-7. PubMed ID: 6859126
[TBL] [Abstract][Full Text] [Related]
11. Two sisters with growth failure, microcephaly, peculiar facies and apical dystrophy: the presentation of brachymorphism-onychodysplasia-dysphalangism syndrome?
Ounap K; Justus I; Lipping-Sitska M
Clin Dysmorphol; 1998 Jan; 7(1):45-50. PubMed ID: 9546830
[TBL] [Abstract][Full Text] [Related]
12. Newly recognized ectrodactyly/deafness syndrome.
Raas-Rothschild A; Aviram A; Ben-Ami T; Berger I; Katznelson MB; Goodman RM
J Craniofac Genet Dev Biol; 1989; 9(2):121-7. PubMed ID: 2794002
[TBL] [Abstract][Full Text] [Related]
13. [A case of congenital hypodactyly of the hand and foot].
Mamedov AG; Seidov MM
Ortop Travmatol Protez; 1991 Apr; (4):51-2. PubMed ID: 1754179
[No Abstract] [Full Text] [Related]
14. Congenital bilateral fibular deficiency with facial dysmorphia, brachydactyly and mental retardation in a girl.
Stoll C; Alembik Y; Repetto M
Genet Couns; 1998; 9(2):147-52. PubMed ID: 9664212
[TBL] [Abstract][Full Text] [Related]
15. Postaxial polydactyly, ulnar ray dysgenesis, and renal cystic dysplasia in sibs.
Kaplan BS; Bellah RD
Am J Med Genet; 1999 Dec; 87(5):426-9. PubMed ID: 10594882
[TBL] [Abstract][Full Text] [Related]
16. Brachydactyly and atrial septal defect: when the digits point to the heart.
Siniorakis E; Arvanitakis S; Tzevelekos P; Mantovani G; Manolakos E; Rentoukas E
Int J Cardiol; 2014 Dec; 177(2):e90-2. PubMed ID: 25456580
[No Abstract] [Full Text] [Related]
17. Rhombencephalosynapsis associated with hand anomalies.
Aydingöz U; Cila A; Aktan G
Br J Radiol; 1997 Jul; 70(835):764-6. PubMed ID: 9245891
[TBL] [Abstract][Full Text] [Related]
18. Minor manifestations in preaxial polydactyly type 1 and Poland complex.
Halal F
Am J Med Genet; 1981; 8(2):221-8. PubMed ID: 7282776
[TBL] [Abstract][Full Text] [Related]
19. Unilateral congenital terminal finger absences: a condition that differs from symbrachydactyly.
Knight JB; Pritsch T; Ezaki M; Oishi SN
J Hand Surg Am; 2012 Jan; 37(1):124-9. PubMed ID: 22051235
[TBL] [Abstract][Full Text] [Related]
20. Unusual cardiac malformations in Holt-Oram syndrome: report of two cases.
Wu JM; Young ML; Wang TR; Lin SJ; Chang JK; Wei J
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1991; 32(2):100-4. PubMed ID: 2063682
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
