217 related articles for article (PubMed ID: 7987310)
21. High-resolution chromosome analysis in autosomal recessive disorders: Laurence-Moon-Bardet-Biedl syndrome.
Fannemel M; Riise R; Lofterød B; Tommerup N
Clin Genet; 1993 Feb; 43(2):111-2. PubMed ID: 8448900
[No Abstract] [Full Text] [Related]
22. Pigmentary retinopathy due to Bardet-Biedl syndrome: case report and literature review.
Andrade LJ; Andrade R; França CS; Bittencourt AV
Arq Bras Oftalmol; 2009; 72(5):694-6. PubMed ID: 20027412
[TBL] [Abstract][Full Text] [Related]
23. [Nosography of the Laurence-Moon-Bardet-Biedl syndrome].
Argenta G; Sadun D; De Giorgio R
Riv Neurol; 1976; 46(2):93-101. PubMed ID: 1006077
[TBL] [Abstract][Full Text] [Related]
24. Hypokalemic paralysis and megaloblastic anaemia in Laurence-Moon-Bardet-Biedl syndrome.
Abbasi A; Butt N; Sultan B; Munir SM
J Coll Physicians Surg Pak; 2009 Mar; 19(3):186-8. PubMed ID: 19268021
[TBL] [Abstract][Full Text] [Related]
25. Laurence-Moon-Biedl syndrome (?) and Prader-Willi syndrome (?) in a single family.
Endo M; Tasaka Y; Matsuura N; Matsuda I
Eur J Pediatr; 1976 Nov; 123(4):269-76. PubMed ID: 991874
[TBL] [Abstract][Full Text] [Related]
26. A pathogenic homozygous variant of the BBS10 gene in a patient with Bardet Biedl syndrome.
Ladino LY; Galvis J; Yasnó D; Ramírez A; Beltrán OI
Biomedica; 2018 Sep; 38(3):308-320. PubMed ID: 30335236
[TBL] [Abstract][Full Text] [Related]
27. Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous.
Leppert M; Baird L; Anderson KL; Otterud B; Lupski JR; Lewis RA
Nat Genet; 1994 May; 7(1):108-12. PubMed ID: 8075632
[TBL] [Abstract][Full Text] [Related]
28. Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigrees.
Katsanis N; Lewis RA; Stockton DW; Mai PM; Baird L; Beales PL; Leppert M; Lupski JR
Am J Hum Genet; 1999 Dec; 65(6):1672-9. PubMed ID: 10577921
[TBL] [Abstract][Full Text] [Related]
29. Dental abnormalities as a component of the Laurence-Moon-Bardet-Biedl syndrome.
Kobrin JL; Ternand CL; Knobloch WH; Johnson DD
Ophthalmic Paediatr Genet; 1990 Dec; 11(4):299-303. PubMed ID: 2096358
[TBL] [Abstract][Full Text] [Related]
30. The cloning and developmental expression of unconventional myosin IXA (MYO9A) a gene in the Bardet-Biedl syndrome (BBS4) region at chromosome 15q22-q23.
Gorman SW; Haider NB; Grieshammer U; Swiderski RE; Kim E; Welch JW; Searby C; Leng S; Carmi R; Sheffield VC; Duhl DM
Genomics; 1999 Jul; 59(2):150-60. PubMed ID: 10409426
[TBL] [Abstract][Full Text] [Related]
31. Laurence-Moon-Bardet-Biedl Syndrome: A Rare Case With a Literature Review.
Kumar A; Husain A; Saleem A; Khawaja UA; Virani S
Cureus; 2020 Nov; 12(11):e11355. PubMed ID: 33304690
[TBL] [Abstract][Full Text] [Related]
32. A further case of Bardet-Biedl syndrome.
Kalangu KK
Cent Afr J Med; 1995 May; 41(5):167-9. PubMed ID: 7628002
[TBL] [Abstract][Full Text] [Related]
33. The possible relationship between Laurence-Moon-Biedl-Bardet syndrome and a schizophrenic-like psychosis.
Weiss M; Meshulam B; Wijsenbeek H
J Nerv Ment Dis; 1981 Apr; 169(4):259-60. PubMed ID: 7217934
[TBL] [Abstract][Full Text] [Related]
34. Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11).
Chiang AP; Beck JS; Yen HJ; Tayeh MK; Scheetz TE; Swiderski RE; Nishimura DY; Braun TA; Kim KY; Huang J; Elbedour K; Carmi R; Slusarski DC; Casavant TL; Stone EM; Sheffield VC
Proc Natl Acad Sci U S A; 2006 Apr; 103(16):6287-92. PubMed ID: 16606853
[TBL] [Abstract][Full Text] [Related]
35. Clinical and molecular characterisation of Bardet-Biedl syndrome in consanguineous populations: the power of homozygosity mapping.
Abu Safieh L; Aldahmesh MA; Shamseldin H; Hashem M; Shaheen R; Alkuraya H; Al Hazzaa SA; Al-Rajhi A; Alkuraya FS
J Med Genet; 2010 Apr; 47(4):236-41. PubMed ID: 19858128
[TBL] [Abstract][Full Text] [Related]
36. Mutation analysis of the MKKS gene in McKusick-Kaufman syndrome and selected Bardet-Biedl syndrome patients.
Slavotinek AM; Searby C; Al-Gazali L; Hennekam RC; Schrander-Stumpel C; Orcana-Losa M; Pardo-Reoyo S; Cantani A; Kumar D; Capellini Q; Neri G; Zackai E; Biesecker LG
Hum Genet; 2002 Jun; 110(6):561-7. PubMed ID: 12107442
[TBL] [Abstract][Full Text] [Related]
37. [The Laurence-Moon-Bardet-Biedl syndrome].
Stefan C; Mercaş V
Oftalmologia; 1994; 38(4):345-7. PubMed ID: 7947672
[TBL] [Abstract][Full Text] [Related]
38. Primary Hypertension as the Presenting Feature of Laurence-Moon-Bardet-Biedl Syndrome: A Report of Two Children.
Thadchanamoorthy V; Jayasekara N; Dayasiri K
Cureus; 2021 Jan; 13(1):e12617. PubMed ID: 33585106
[TBL] [Abstract][Full Text] [Related]
39. Tibia vara in a patient with Bardet-Biedl syndrome.
Motzkin NE; Bianco AJ; Zimmerman D
Mayo Clin Proc; 1992 Jun; 67(6):549-52. PubMed ID: 1434882
[TBL] [Abstract][Full Text] [Related]
40. Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3).
Chiang AP; Nishimura D; Searby C; Elbedour K; Carmi R; Ferguson AL; Secrist J; Braun T; Casavant T; Stone EM; Sheffield VC
Am J Hum Genet; 2004 Sep; 75(3):475-84. PubMed ID: 15258860
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
