113 related articles for article (PubMed ID: 7815449)
21. Acrocallosal syndrome in two African brothers born to consanguineous parents.
Christianson AL; Venter PA; Du Toit JL; Shipalana N; Gericke GS
Am J Med Genet; 1994 Jun; 51(2):98-101. PubMed ID: 8092201
[TBL] [Abstract][Full Text] [Related]
22. Polydactyly, campomelia, ambiguous genitalia, cystic dysplastic kidneys, and cerebral malformation in a fetus of consanguineous parents: a new multiple malformation syndrome, or a severe form of oral-facial-digital syndrome type IV?
Adès LC; Clapton WK; Morphett A; Morris LL; Haan EA
Am J Med Genet; 1994 Jan; 49(2):211-7. PubMed ID: 8116671
[TBL] [Abstract][Full Text] [Related]
23. Anterior segment anomalies of the eye associated with multiple skeletal abnormalities and early lethality: confirmation of an autosomal recessive syndrome.
al-Gazali LI; Bakir M; Sadaghatian MR; Nath R; Haas D
Clin Dysmorphol; 1999 Apr; 8(2):87-92. PubMed ID: 10319196
[TBL] [Abstract][Full Text] [Related]
24. Autosomal dominant polycystic kidney disease diagnosed in utero. Review.
Nowak M; Huras H; Wiecheć M; Jach R; Radoń-Pokracka M; Górecka J
Ginekol Pol; 2016; 87(8):605-8. PubMed ID: 27629138
[TBL] [Abstract][Full Text] [Related]
25. Polycystic kidneys associated with malformations of the brain, polydactyly, and other birth defects in newborn sibs. A lethal syndrome showing the autosomal-recessive pattern of inheritance.
Fried K; Liban E; Lurie M; Friedman S; Reisner SH
J Med Genet; 1971 Sep; 8(3):285-90. PubMed ID: 4999589
[No Abstract] [Full Text] [Related]
26. Beemer-Langer type short rib-polydactyly syndrome: report of two cases.
Tsai FJ; Tsai CH; Wang TR
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1994; 35(4):331-4. PubMed ID: 8085456
[TBL] [Abstract][Full Text] [Related]
27. Cerebro-reno-digital syndrome in two sibs.
Piantanida M; Tiberti A; Plebani A; Martelli P; Danesino C
Am J Med Genet; 1993 Sep; 47(3):420-2. PubMed ID: 8135292
[TBL] [Abstract][Full Text] [Related]
28. Genetic heterogeneity of Meckel syndrome.
Roume J; Ma HW; Le Merrer M; Cormier-Daire V; Girlich D; Genin E; Munnich A
J Med Genet; 1997 Dec; 34(12):1003-6. PubMed ID: 9429143
[TBL] [Abstract][Full Text] [Related]
29. GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome.
Kang S; Graham JM; Olney AH; Biesecker LG
Nat Genet; 1997 Mar; 15(3):266-8. PubMed ID: 9054938
[TBL] [Abstract][Full Text] [Related]
30. A hypomorphic allele reveals an important role of inturned in mouse skeletal development.
Chang R; Petersen JR; Niswander LA; Liu A
Dev Dyn; 2015 Jun; 244(6):736-47. PubMed ID: 25774014
[TBL] [Abstract][Full Text] [Related]
31. Acrofacial dysostosis in a patient with the TSC2-PKD1 contiguous gene syndrome.
Dauwerse JG; Bouman K; van Essen AJ; van Der Hout AH; Kolsters G; Breuning MH; Peters DJ
J Med Genet; 2002 Feb; 39(2):136-41. PubMed ID: 11836366
[No Abstract] [Full Text] [Related]
32. 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]
33. Clinical anophthalmia, dextrocardia, and skeletal anomalies in an infant born to consanguineous parents.
Aughton DJ
Am J Med Genet; 1990 Oct; 37(2):178-81. PubMed ID: 2248283
[No Abstract] [Full Text] [Related]
34. Associated malformations in the family of a patient with Meckel syndrome: heterozygous expression?
Gulati R; Phadke SR; Agarwal SS
J Med Genet; 1997 Nov; 34(11):937-8. PubMed ID: 9391891
[TBL] [Abstract][Full Text] [Related]
35. A further case of a new syndrome including midface retraction, hypertrichosis, and skeletal anomalies.
Donnai D; Harris R
J Med Genet; 1979 Dec; 16(6):483-6. PubMed ID: 537022
[TBL] [Abstract][Full Text] [Related]
36. Autosomal dominant polycystic kidney disease in the first year of life. Report of a case with no family history.
Stalens JP; Sokal E; Walon C; Verellen-Dumoulin C; Clapuyt P; Wese FX
Acta Urol Belg; 1993 Dec; 61(4):25-8. PubMed ID: 8296686
[TBL] [Abstract][Full Text] [Related]
37. Cerebro-oculo-facio-skeletal (COFS) syndrome in siblings.
Kulkarni ML; Sehgal A; Keshavamurthy KS; Kulkarni PM
Indian J Pediatr; 2004 Dec; 71(12):e56-7. PubMed ID: 15630331
[TBL] [Abstract][Full Text] [Related]
38. Jeune syndrome with tongue lobulation and preaxial polydactyly, and Jeune syndrome with situs inversus and asplenia: compound heterozygosity Jeune-Mohr and Jeune-Ivemark?
Majewski E; Oztürk B; Gillessen-Kaesbach G
Am J Med Genet; 1996 May; 63(1):74-9. PubMed ID: 8723090
[TBL] [Abstract][Full Text] [Related]
39. Achondrogenesis type II with polydactyly.
Rittler M; Orioli IM
Am J Med Genet; 1995 Nov; 59(2):157-60. PubMed ID: 8588578
[TBL] [Abstract][Full Text] [Related]
40. [Bone malformations associated with deletion of the long arm of chromosome X].
Hurgoiu V; Suciu S; Nicoară Z; Florescu P; David-Mark S
Rev Pediatr Obstet Ginecol Pediatr; 1988; 37(4):373-6. PubMed ID: 3150606
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]