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Results: 1 to 20 of 123

1.

Watson syndrome: is it a subtype of type 1 neurofibromatosis?

Allanson JE, Upadhyaya M, Watson GH, Partington M, MacKenzie A, Lahey D, MacLeod H, Sarfarazi M, Broadhead W, Harper PS, et al.

J Med Genet. 1991 Nov;28(11):752-6.

PMID:
1770531
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Evidence of central nervous system involvement in Watson syndrome.

Leão M, da Silva ML.

Pediatr Neurol. 1995 Apr;12(3):252-4.

PMID:
7619195
[PubMed - indexed for MEDLINE]
3.

Tandem duplication within a neurofibromatosis type 1 (NF1) gene exon in a family with features of Watson syndrome and Noonan syndrome.

Tassabehji M, Strachan T, Sharland M, Colley A, Donnai D, Harris R, Thakker N.

Am J Hum Genet. 1993 Jul;53(1):90-5.

PMID:
8317503
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Noonan syndrome with café-au-lait spots and multiple lentigines syndrome are not linked to the neurofibromatosis type 1 locus.

Ahlbom BE, Dahl N, Zetterqvist P, Annerén G.

Clin Genet. 1995 Aug;48(2):85-9.

PMID:
7586657
[PubMed - indexed for MEDLINE]
5.

Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: evidence of non-linkage.

Charrow J, Listernick R, Ward K.

Am J Med Genet. 1993 Mar 1;45(5):606-8.

PMID:
8456833
[PubMed - indexed for MEDLINE]
6.

A genetic study of neurofibromatosis type 1 (NF1) in south-western Ontario. II. A PCR based approach to molecular and prenatal diagnosis using linkage.

Rodenhiser DI, Ainsworth PJ, Coulter-Mackie MB, Singh SM, Jung JH.

J Med Genet. 1993 May;30(5):363-8.

PMID:
8320697
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Genetic linkage mapping of chromosome 17 markers and neurofibromatosis type I.

Vance JM, Pericak-Vance MA, Yamaoka LH, Speer MC, Rosenwasser GO, Small K, Gaskell PC Jr, Hung WY, Alberts MJ, Haynes CS, et al.

Am J Hum Genet. 1989 Jan;44(1):25-9.

PMID:
2491777
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Hereditary spinal neurofibromatosis: a rare form of NF1?

Poyhonen M, Leisti EL, Kytölä S, Leisti J.

J Med Genet. 1997 Mar;34(3):184-7.

PMID:
9132486
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locus.

Sharland M, Taylor R, Patton MA, Jeffery S.

J Med Genet. 1992 Mar;29(3):188-90.

PMID:
1348095
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Pulmonary artery aneurysm and coronary artery disease in the clinical presentation of watson syndrome.

Foster JL, Bradley SM, Ikonomidis JS.

Ann Thorac Surg. 2006 Aug;82(2):740-2.

PMID:
16863806
[PubMed - indexed for MEDLINE]
11.

An EcoRI RFLP in the 5' region of the human NF1 gene.

Reyniers E, De Boulle K, Marchuk DA, Andersen LB, Collins FS, Willems PJ.

Hum Genet. 1993 Dec;92(6):631.

PMID:
7903272
[PubMed - indexed for MEDLINE]
12.

Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?

Stern HJ, Saal HM, Lee JS, Fain PR, Goldgar DE, Rosenbaum KN, Barker DF.

J Med Genet. 1992 Mar;29(3):184-7.

PMID:
1348094
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Exclusion of the neurofibromatosis 1 locus in a family with inherited café-au-lait spots.

Brunner HG, Hulsebos T, Steijlen PM, der Kinderen DJ, vd Steen A, Hamel BC.

Am J Med Genet. 1993 Jun 1;46(4):472-4.

PMID:
8357027
[PubMed - indexed for MEDLINE]
14.

[From gene to disease; neurofibromatosis type 1].

de Goede-Bolder A, Cnossen MH, Dooijes D, van den Ouweland AM, Niermeijer MF.

Ned Tijdschr Geneeskd. 2001 Sep 8;145(36):1736-8. Review. Dutch.

PMID:
11572174
[PubMed - indexed for MEDLINE]
15.

[Plexiform neurofibroma and basal ganglia anomaly in Watson syndrome].

Weber P, Kotthoff S, Schuierer G, Kurlemann G.

Klin Padiatr. 1999 May-Jun;211(3):172-4. German.

PMID:
10412128
[PubMed - indexed for MEDLINE]
16.

Close flanking markers for neurofibromatosis type I (NF1).

Upadhyaya M, Sarfarazi M, Huson SM, Broadhead W, Fryer A, Harper PS.

Am J Hum Genet. 1989 Jan;44(1):41-7.

PMID:
2491781
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

The different forms of neurofibromatosis.

Ruggieri M.

Childs Nerv Syst. 1999 Jul;15(6-7):295-308. Review.

PMID:
10461778
[PubMed - indexed for MEDLINE]
18.

Familial café au lait spots: a variant of neurofibromatosis type 1.

Abeliovich D, Gelman-Kohan Z, Silverstein S, Lerer I, Chemke J, Merin S, Zlotogora J.

J Med Genet. 1995 Dec;32(12):985-6.

PMID:
8825931
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

A clinical variant of neurofibromatosis type 1: familial spinal neurofibromatosis with a frameshift mutation in the NF1 gene.

Ars E, Kruyer H, Gaona A, Casquero P, Rosell J, Volpini V, Serra E, Lázaro C, Estivill X.

Am J Hum Genet. 1998 Apr;62(4):834-41.

PMID:
9529361
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis association.

Bahuau M, Flintoff W, Assouline B, Lyonnet S, Le Merrer M, Prieur M, Guilloud-Bataille M, Feingold N, Munnich A, Vidaud M, Vidaud D.

Am J Med Genet. 1996 Dec 18;66(3):347-55.

PMID:
8985499
[PubMed - indexed for MEDLINE]

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