208 related articles for article (PubMed ID: 3189394)
1. Autosomal recessive Robinow-like syndrome with anterior chamber cleavage anomalies.
Saal HM; Greenstein RM; Weinbaum PJ; Poole AE
Am J Med Genet; 1988 Jul; 30(3):709-18. PubMed ID: 3189394
[TBL] [Abstract][Full Text] [Related]
2. Autosomal recessive Robinow syndrome.
Teebi AS
Am J Med Genet; 1990 Jan; 35(1):64-8. PubMed ID: 2301471
[TBL] [Abstract][Full Text] [Related]
3. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: a new autosomal recessive syndrome.
Richieri-Costa A; Pereira SC
Am J Med Genet; 1992 Mar; 42(5):681-7. PubMed ID: 1632438
[TBL] [Abstract][Full Text] [Related]
4. Sibs with Axenfeld-Rieger anomaly, hydrocephalus, and leptomeningeal calcifications: a new autosomal recessive syndrome?
Moog U; Bleeker-Wagemakers EM; Crobach P; Vles JS; Schrander-Stumpel CT
Am J Med Genet; 1998 Jul; 78(3):263-6. PubMed ID: 9677063
[TBL] [Abstract][Full Text] [Related]
5. A child with sclerocornea, short limbs, short stature, and distinct facial appearance.
Thompson EM; Winter RM
Am J Med Genet; 1988 Jul; 30(3):719-24. PubMed ID: 3055984
[TBL] [Abstract][Full Text] [Related]
6. Congenital scalp skull defects with distal limb anomalies (Adams-Oliver syndrome--McKusick 10030): further suggestion of autosomal recessive inheritance.
Koiffmann CP; Wajntal A; Huyke BJ; Castro RM
Am J Med Genet; 1988 Feb; 29(2):263-8. PubMed ID: 3354597
[TBL] [Abstract][Full Text] [Related]
7. Orofacial manifestations of Robinow's syndrome: a case report in a pediatric patient.
Cerqueira DF; de Souza IP
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2008 Mar; 105(3):353-7. PubMed ID: 18061493
[TBL] [Abstract][Full Text] [Related]
8. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
Bonioli E; Palmieri A; Bertola A; Bellini C
Genet Couns; 1995; 6(4):309-12. PubMed ID: 8775417
[TBL] [Abstract][Full Text] [Related]
9. Autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfeet in male patients.
Richieri-Costa A; Pereira SC
Am J Med Genet; 1993 Oct; 47(5):707-9. PubMed ID: 8267000
[TBL] [Abstract][Full Text] [Related]
10. Congenital hypothyroidism in Peters plus syndrome.
Kosaki R; Kamiishi A; Sugiyama R; Kawai M; Hasegawa T; Kosaki K
Ophthalmic Genet; 2006 Jun; 27(2):67-9. PubMed ID: 16754209
[TBL] [Abstract][Full Text] [Related]
11. Provisionally unique autosomal recessive chondrodysplasia punctata syndrome.
Toriello HV; Higgins JV; Miller T
Am J Med Genet; 1993 Oct; 47(5):797-9. PubMed ID: 8267015
[TBL] [Abstract][Full Text] [Related]
12. Limb reduction defects and renal dysplasia: confirmation of a new, apparently lethal, autosomal recessive MCA syndrome.
Schrander-Stumpel C; de Die-Smulders C; Fryns JP; da Costa J; Bouckaert P
Am J Med Genet; 1990 Sep; 37(1):133-5. PubMed ID: 2240030
[TBL] [Abstract][Full Text] [Related]
13. Corpus callosum agenesis, facial anomalies, Robin sequence, and other anomalies: a new autosomal recessive syndrome?
Toriello HV; Carey JC
Am J Med Genet; 1988 Sep; 31(1):17-23. PubMed ID: 3223497
[TBL] [Abstract][Full Text] [Related]
14. PHAVER syndrome: an autosomal recessive syndrome of limb pterygia, congenital heart anomalies, vertebral defects, ear anomalies, and radial defects.
Powell CM; Chandra RS; Saal HM
Am J Med Genet; 1993 Nov; 47(6):807-11. PubMed ID: 8279476
[TBL] [Abstract][Full Text] [Related]
15. Probable Marden-Walker syndrome: evidence for autosomal recessive inheritance.
Temtamy SA; Shoukry AS; Raafat M; Mihareb S
Birth Defects Orig Artic Ser; 1975; 11(2):104-8. PubMed ID: 1227520
[TBL] [Abstract][Full Text] [Related]
16. Mesomelic limb shortness: a previously unreported autosomal recessive type.
Reardon W; Hall CM; Slaney S; Huson SM; Connell J; al-Hilaly N; Fixsen J; Baraitser M; Winter RM
Am J Med Genet; 1993 Oct; 47(5):788-92. PubMed ID: 8267013
[TBL] [Abstract][Full Text] [Related]
17. Dandy-Walker(like) malformation, atrio-ventricular septal defect and a similar pattern of minor anomalies in 2 sisters: a new syndrome?
Ritscher D; Schinzel A; Boltshauser E; Briner J; Arbenz U; Sigg P
Am J Med Genet; 1987 Feb; 26(2):481-91. PubMed ID: 3812597
[TBL] [Abstract][Full Text] [Related]
18. Two unrelated children with developmental delay, short stature and anterior chamber cleavage disorder, cerebellar hypoplasia, endocrine disturbances and tracheostenosis: a new entity?
Jung C; Wolff G; Back E; Stahl M
Clin Dysmorphol; 1995 Jan; 4(1):44-51. PubMed ID: 7537583
[TBL] [Abstract][Full Text] [Related]
19. Brief clinical report: HARD (+/- E) syndrome: report of a sixth family with support for autosomal-recessive inheritance.
Aymé S; Mattei JF
Am J Med Genet; 1983 Apr; 14(4):759-66. PubMed ID: 6405616
[TBL] [Abstract][Full Text] [Related]
20. Report of a case and further delineation of the SHORT syndrome.
Toriello HV; Wakefield S; Komar K; Higgins JV; Waterman DF
Am J Med Genet; 1985 Oct; 22(2):311-4. PubMed ID: 4050863
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
