137 related articles for article (PubMed ID: 1981029)
1. Prenatal diagnosis of the neurofibromatoses.
Pulst SM
Clin Perinatol; 1990 Dec; 17(4):829-44. PubMed ID: 1981029
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 8320697
[TBL] [Abstract][Full Text] [Related]
3. [Neurofibromatosis--new clinical and molecular genetic aspects].
Froster-Iskenius UG; Wolff HH
Hautarzt; 1991 May; 42(5):279-83. PubMed ID: 1678737
[TBL] [Abstract][Full Text] [Related]
4. [Neurofibromatosis: current clinical and molecular genetic aspects from the neurologic viewpoint].
Mautner VF; Laute S; Schneider E; Pulst SM
Nervenarzt; 1991 Jun; 62(6):340-8. PubMed ID: 1678877
[TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of neurofibromatosis type 1: from flanking RFLPs to intragenic microsatellite markers.
Lazaro C; Gaona A; Ravella A; Volpini V; Estivill X
Prenat Diagn; 1995 Feb; 15(2):129-34. PubMed ID: 7784363
[TBL] [Abstract][Full Text] [Related]
6. The Genoa experience of prenatal diagnosis in NF1.
Origone P; Bonioli E; Panucci E; Costabel S; Ajmar F; Coviello DA
Prenat Diagn; 2000 Sep; 20(9):719-24. PubMed ID: 11015700
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis and presymptomatic detection of neurofibromatosis type 1.
Upadhyaya M; Fryer A; MacMillan J; Broadhead W; Huson SM; Harper PS
J Med Genet; 1992 Mar; 29(3):180-3. PubMed ID: 1348093
[TBL] [Abstract][Full Text] [Related]
8. Reproductive decisions after prenatal diagnosis in neurofibromatosis type 1: importance of genetic counseling.
Terzi YK; Oguzkan-Balci S; Anlar B; Aysun S; Guran S; Ayter S
Genet Couns; 2009; 20(2):195-202. PubMed ID: 19650418
[TBL] [Abstract][Full Text] [Related]
9. Diagnosis of neurofibromatosis type 1 using RFLPs tightly linked to gene.
Vivarelli R; Bartalani G; Berardi A; Calistri L; Balestri P; Fois A
Childs Nerv Syst; 1993 Jun; 9(3):147-9. PubMed ID: 8104099
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of neurofibromatosis type 1: sonographic and MRI findings.
McEwing RL; Joelle R; Mohlo M; Bernard JP; Hillion Y; Ville Y
Prenat Diagn; 2006 Dec; 26(12):1110-4. PubMed ID: 16981221
[TBL] [Abstract][Full Text] [Related]
11. Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy.
Meredith AL; Huson SM; Lunt PW; Sarfarazi M; Harley HG; Brook JD; Shaw DJ; Harper PS
Br Med J (Clin Res Ed); 1986 Nov; 293(6558):1353-6. PubMed ID: 2878705
[TBL] [Abstract][Full Text] [Related]
12. Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22.
Rouleau GA; Wertelecki W; Haines JL; Hobbs WJ; Trofatter JA; Seizinger BR; Martuza RL; Superneau DW; Conneally PM; Gusella JF
Nature; 1987 Sep 17-23; 329(6136):246-8. PubMed ID: 2888021
[TBL] [Abstract][Full Text] [Related]
13. Central neurofibromatosis with bilateral acoustic neuroma.
Eldridge R
Adv Neurol; 1981; 29():57-65. PubMed ID: 6798843
[No Abstract] [Full Text] [Related]
14. Prenatal diagnosis of sporadic neurofibromatosis type 1 (NF1) by RNA and DNA analysis of a splicing mutation.
Ars E; Kruyer H; Gaona A; Serra E; Lázaro C; Estivill X
Prenat Diagn; 1999 Aug; 19(8):739-42. PubMed ID: 10451518
[TBL] [Abstract][Full Text] [Related]
15. [The prenatal diagnosis of hemophilia A--the use of PCR and family RFLP analysis].
Bian M
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1993 Apr; 15(2):102-7. PubMed ID: 7902217
[TBL] [Abstract][Full Text] [Related]
16. Prenatal exclusion of Norrie's disease.
Redmond RM; Graham CA; Kelly ED; Coleman M; Nevin NC
Br J Ophthalmol; 1992 Aug; 76(8):491-3. PubMed ID: 1390533
[TBL] [Abstract][Full Text] [Related]
17. Central neurofibromatosis with bilateral acoustic neuroma: genetic, clinical and biochemical distinctions from peripheral neurofibromatosis.
Kanter WR; Eldridge R; Fabricant R; Allen JC; Koerber T
Neurology; 1980 Aug; 30(8):851-9. PubMed ID: 6774282
[TBL] [Abstract][Full Text] [Related]
18. [Clinical molecular-genetics for endocrine and metabolic diseases].
Niikawa N
Rinsho Byori; 1989 Aug; 37(8):847-54. PubMed ID: 2573745
[TBL] [Abstract][Full Text] [Related]
19. RFLPs of 21-hydroxylase and C4 genes: application to pedigree analysis on 21-hydroxylase deficiency.
Matsumoto T; Kondoh T; Baba T; Yoshimoto M; Niikawa N; Tsuji Y
Acta Paediatr Jpn; 1988; 30 Suppl():111-6. PubMed ID: 2906201
[No Abstract] [Full Text] [Related]
20. [Neurofibromatosis; genetic and clinical aspects].
Fleury P
Ned Tijdschr Geneeskd; 1989 Nov; 133(46):2279-83. PubMed ID: 2511452
[No Abstract] [Full Text] [Related]
[Next] [New Search]
