158 related articles for article (PubMed ID: 11810276)
1. Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome.
Kelberman D; Tyson J; Chandler DC; McInerney AM; Slee J; Albert D; Aymat A; Botma M; Calvert M; Goldblatt J; Haan EA; Laing NG; Lim J; Malcolm S; Singer SL; Winter RM; Bitner-Glindzicz M
Hum Genet; 2001 Dec; 109(6):638-45. PubMed ID: 11810276
[TBL] [Abstract][Full Text] [Related]
2. Auriculo-condylar syndrome: mapping of a first locus and evidence for genetic heterogeneity.
Masotti C; Oliveira KG; Poerner F; Splendore A; Souza J; Freitas Rda S; Zechi-Ceide R; Guion-Almeida ML; Passos-Bueno MR
Eur J Hum Genet; 2008 Feb; 16(2):145-52. PubMed ID: 18000524
[TBL] [Abstract][Full Text] [Related]
3. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
Lin MW; Lee DD; Lin CH; Huang CY; Wong CK; Chang YT; Liu HN; Hsiao KJ; Tsai SF
Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797
[TBL] [Abstract][Full Text] [Related]
4. Search for genes involved in Joubert syndrome: evidence that one or more major loci are yet to be identified and exclusion of candidate genes EN1, EN2, FGF8, and BARHL1.
Blair IP; Gibson RR; Bennett CL; Chance PF
Am J Med Genet; 2002 Jan; 107(3):190-6. PubMed ID: 11807898
[TBL] [Abstract][Full Text] [Related]
5. A new locus for Seckel syndrome on chromosome 18p11.31-q11.2.
Børglum AD; Balslev T; Haagerup A; Birkebaek N; Binderup H; Kruse TA; Hertz JM
Eur J Hum Genet; 2001 Oct; 9(10):753-7. PubMed ID: 11781686
[TBL] [Abstract][Full Text] [Related]
6. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
7. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
Winkelmann J; Lichtner P; Pütz B; Trenkwalder C; Hauk S; Meitinger T; Strom T; Muller-Myhsok B
Mov Disord; 2006 Jan; 21(1):28-33. PubMed ID: 16124010
[TBL] [Abstract][Full Text] [Related]
8. A novel locus for Meckel-Gruber syndrome, MKS3, maps to chromosome 8q24.
Morgan NV; Gissen P; Sharif SM; Baumber L; Sutherland J; Kelly DA; Aminu K; Bennett CP; Woods CG; Mueller RF; Trembath RC; Maher ER; Johnson CA
Hum Genet; 2002 Oct; 111(4-5):456-61. PubMed ID: 12384791
[TBL] [Abstract][Full Text] [Related]
9. Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?
Lohmann-Hedrich K; Neumann A; Kleensang A; Lohnau T; Muhle H; Djarmati A; König IR; Pramstaller PP; Schwinger E; Kramer PL; Ziegler A; Stephani U; Klein C
Neurology; 2008 Feb; 70(9):686-94. PubMed ID: 18032746
[TBL] [Abstract][Full Text] [Related]
10. Linkage of one gene for familial glucocorticoid deficiency type 2 (FGD2) to chromosome 8q and further evidence of heterogeneity.
Génin E; Huebner A; Jaillard C; Faure A; Halaby G; Saka N; Clark AJ; Durand P; Bégeot M; Naville D
Hum Genet; 2002 Oct; 111(4-5):428-34. PubMed ID: 12384787
[TBL] [Abstract][Full Text] [Related]
11. Linkage analysis narrows the critical region for oculodentodigital dysplasia to chromosome 6q22-q23.
Boyadjiev SA; Jabs EW; LaBuda M; Jamal JE; Torbergsen T; Ptácek LJ; Rogers RC; Nyberg-Hansen R; Opjordsmoen S; Zeller CB; Stine OC; Stalker HJ; Zori RT; Shapiro RE
Genomics; 1999 May; 58(1):34-40. PubMed ID: 10331943
[TBL] [Abstract][Full Text] [Related]
12. Autosomal dominant infantile gastroesophageal reflux disease: exclusion of a 13q14 locus in five well characterized families.
Orenstein SR; Shalaby TM; Finch R; Pfuetzer RH; DeVandry S; Chensny LJ; Bannada MM; Whitcomb DC
Am J Gastroenterol; 2002 Nov; 97(11):2725-32. PubMed ID: 12425539
[TBL] [Abstract][Full Text] [Related]
13. Familial hemifacial microsomia.
Taysi K; Marsh JL; Wise DM
Cleft Palate J; 1983 Jan; 20(1):47-53. PubMed ID: 6572575
[TBL] [Abstract][Full Text] [Related]
14. Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3.
Hedera P; Blair MA; Andermann E; Andermann F; D'Agostino D; Taylor KA; Chahine L; Pandolfo M; Bradford Y; Haines JL; Abou-Khalil B
Neurology; 2007 Jun; 68(24):2107-12. PubMed ID: 17377072
[TBL] [Abstract][Full Text] [Related]
15. Hemifacial microsomia and the branchio-oto-renal syndrome.
Rollnick BR; Kaye CI
J Craniofac Genet Dev Biol Suppl; 1985; 1():287-95. PubMed ID: 3877103
[TBL] [Abstract][Full Text] [Related]
16. Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large family.
Legius E; Schollen E; Matthijs G; Fryns JP
Eur J Hum Genet; 1998 Jan; 6(1):32-7. PubMed ID: 9781012
[TBL] [Abstract][Full Text] [Related]
17. Genetic heterogeneity of syndromic X-linked recessive microphthalmia-anophthalmia: is Lenz microphthalmia a single disorder?
Ng D; Hadley DW; Tifft CJ; Biesecker LG
Am J Med Genet; 2002 Jul; 110(4):308-14. PubMed ID: 12116202
[TBL] [Abstract][Full Text] [Related]
18. Fifth finger camptodactyly maps to chromosome 3q11.2-q13.12 in a large German kindred.
Malik S; Schott J; Schiller J; Junge A; Baum E; Koch MC
Eur J Hum Genet; 2008 Feb; 16(2):265-9. PubMed ID: 18000522
[TBL] [Abstract][Full Text] [Related]
19. Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22.
Lambert D; Middle F; Hamshere ML; Segurado R; Raybould R; Corvin A; Green E; O'Mahony E; Nikolov I; Mulcahy T; Haque S; Bort S; Bennett P; Norton N; Owen MJ; Kirov G; Lendon C; Jones L; Jones I; Holmans P; Gill M; Craddock N
Mol Psychiatry; 2005 Sep; 10(9):831-41. PubMed ID: 15940300
[TBL] [Abstract][Full Text] [Related]
20. An autosomal genome-wide screen for celiac disease in Bedouin families.
Ding YC; Weizman Z; Yerushalmi B; Elbedour K; Garner CP; Neuhausen SL
Genes Immun; 2008 Jan; 9(1):81-6. PubMed ID: 17943142
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]