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4. Nonspecific X-linked mental retardation I: a review with information from 24 new families. Herbst DS Am J Med Genet; 1980; 7(4):443-60. PubMed ID: 7011032 [TBL] [Abstract][Full Text] [Related]
5. Craniosynostosis and syndromes with craniosynostosis: incidence, genetics, penetrance, variability, and new syndrome updating. Cohen MM Birth Defects Orig Artic Ser; 1979; 15(5B):13-63. PubMed ID: 393319 [No Abstract] [Full Text] [Related]
6. Macrosomia and mental retardation: evidence of autosomal dominant inheritance in four generations. Mangano L; Palmeri S; Dotti MT; Moschini F; Federico A Am J Med Genet; 1989 Jan; 32(1):67-71. PubMed ID: 2705485 [TBL] [Abstract][Full Text] [Related]
8. Noonan phenotype associated with neurofibromatosis. Allanson JE; Hall JG; Van Allen MI Am J Med Genet; 1985 Jul; 21(3):457-62. PubMed ID: 2411134 [TBL] [Abstract][Full Text] [Related]
9. [Genetic counseling in neurofibromatosis. Apropos of a study of 53 families]. Toutain A; Kaplan J; Briard ML; Frézal J J Genet Hum; 1988 Jun; 36(3):163-71. PubMed ID: 3137311 [TBL] [Abstract][Full Text] [Related]
11. [Genealogical analysis of dominant mutation in neurofibromatosis (Recklinghausen's disease)]. Sergeev AS Genetika; 1973 Nov; 9(11):153-8. PubMed ID: 4219927 [No Abstract] [Full Text] [Related]
12. The pathophysiology of neurofibromatosis: IX. Paternal age as a factor in the origin of new mutations. Riccardi VM; Dobson CE; Chakraborty R; Bontke C Am J Med Genet; 1984 May; 18(1):169-76. PubMed ID: 6430086 [TBL] [Abstract][Full Text] [Related]
13. Neurofibromatosis: variable expression is not intrinsic to the mutant gene. Riccardi VM; Kleiner B; Lubs ML Birth Defects Orig Artic Ser; 1979; 15(5B):283-9. PubMed ID: 118781 [No Abstract] [Full Text] [Related]
14. 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]
15. Recurrence of holoprosencephaly in families with a positive history. Benke PJ; Cohen MM Clin Genet; 1983 Nov; 24(5):324-8. PubMed ID: 6652942 [TBL] [Abstract][Full Text] [Related]
16. X-linked mental retardation with heterozygous expression and macrocephaly: pericentromeric gene localization. Turner G; Gedeon A; Mulley J Am J Med Genet; 1994 Jul; 51(4):575-80. PubMed ID: 7943042 [TBL] [Abstract][Full Text] [Related]
17. Paternal origin of new mutations in von Recklinghausen neurofibromatosis. Jadayel D; Fain P; Upadhyaya M; Ponder MA; Huson SM; Carey J; Fryer A; Mathew CG; Barker DF; Ponder BA Nature; 1990 Feb; 343(6258):558-9. PubMed ID: 2105472 [TBL] [Abstract][Full Text] [Related]
18. Segregation analysis in nonsyndromic holoprosencephaly. Odent S; Le Marec B; Munnich A; Le Merrer M; Bonaïti-Pellié C Am J Med Genet; 1998 May; 77(2):139-43. PubMed ID: 9605287 [TBL] [Abstract][Full Text] [Related]
19. The spectrum of "complicated spastic paraplegia, MASA syndrome and X-linked hydrocephalus". Contribution of DNA linkage analysis in genetic counseling of individual families. Schrander-Stumpel C; Meyer H; Merckx D; Jones M; Israel J; Sommer A; Stevens C; Tinschert S; Wilson G; Willems P Genet Couns; 1994; 5(1):1-10. PubMed ID: 8031529 [TBL] [Abstract][Full Text] [Related]
20. Paternal age and sporadic neurofibromatosis 1: a case-control study and consideration of the methodologic issues. Bunin GR; Needle M; Riccardi VM Genet Epidemiol; 1997; 14(5):507-16. PubMed ID: 9358268 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]