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2. Significant difference of opinion regarding the role of noggin in fibrodysplasia ossificans progressiva. Warman ML Am J Med Genet; 2002 Apr; 109(2):162; author reply 163-4. PubMed ID: 11977169 [No Abstract] [Full Text] [Related]
3. A new mutation of the noggin gene in a French Fibrodysplasia ossificans progressiva (FOP) family. Fontaine K; Sémonin O; Legarde JP; Lenoir G; Lucotte G Genet Couns; 2005; 16(2):149-54. PubMed ID: 16080294 [TBL] [Abstract][Full Text] [Related]
4. A de novo heterozygous deletion of 42 base-pairs in the noggin gene of a fibrodysplasia ossificans progressiva patient. Lucotte G; Sémonin O; Lutz P Clin Genet; 1999 Dec; 56(6):469-70. PubMed ID: 10665670 [No Abstract] [Full Text] [Related]
5. Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP). Xu MQ; Feldman G; Le Merrer M; Shugart YY; Glaser DL; Urtizberea JA; Fardeau M; Connor JM; Triffitt J; Smith R; Shore EM; Kaplan FS Clin Genet; 2000 Oct; 58(4):291-8. PubMed ID: 11076054 [TBL] [Abstract][Full Text] [Related]
6. Bone morphogenetic proteins with some comments on fibrodysplasia ossificans progressiva and NOGGIN. Cohen MM Am J Med Genet; 2002 Apr; 109(2):87-92. PubMed ID: 11977155 [No Abstract] [Full Text] [Related]
7. The tale of FOP, NOGGIN and myristoylation: no data, no proof! Seemann P; Mundlos S Genet Couns; 2008; 19(3):353-5; author reply 361-3. PubMed ID: 18990992 [No Abstract] [Full Text] [Related]
8. Mutations of the noggin and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP). Lucotte G; Lagarde JP; Genet Couns; 2007; 18(3):349-52. PubMed ID: 18019378 [No Abstract] [Full Text] [Related]
9. Response to "Mutations of the NOGGIN and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP)" by Lucotte et al. Kaplan FS; Xu M; Feldman G; Brown M; Cho TJ; Choi IH; Connor JM; Delai PL; Economides AN; Glaser DL; Groppe J; Katagiri T; Le Merrer M; Morhart R; Ravazzolo R; Rogers JG; Smith R; Triffitt JT; Urtizberea JA; Zasloff M; Shore EM Genet Couns; 2008; 19(3):357-9; author reply 361-3. PubMed ID: 18990993 [No Abstract] [Full Text] [Related]
10. Single-molecule PCR: an artifact-free PCR approach for the analysis of somatic mutations. Kraytsberg Y; Khrapko K Expert Rev Mol Diagn; 2005 Sep; 5(5):809-15. PubMed ID: 16149882 [TBL] [Abstract][Full Text] [Related]
12. Identification of three novel mutations of the noggin gene in patients with fibrodysplasia ossificans progressiva. Sémonin O; Fontaine K; Daviaud C; Ayuso C; Lucotte G Am J Med Genet; 2001 Sep; 102(4):314-7. PubMed ID: 11503156 [TBL] [Abstract][Full Text] [Related]
13. Mutations of the noggin (NOG) and of the activin A type I receptor (ACVR1) genes in a series of twenty-seven French fibrodysplasia ossificans progressiva (FOP) patients. Lucotte G; Houzet A; Hubans C; Lagarde JP; Lenoir G Genet Couns; 2009; 20(1):53-62. PubMed ID: 19400542 [TBL] [Abstract][Full Text] [Related]
14. Detection of plasmid contamination in PCR samples. Nerenberg MI; Minor T Biotechniques; 1991 Sep; 11(3):332, 335. PubMed ID: 1931032 [No Abstract] [Full Text] [Related]
15. Significance of real-time quantitative PCR detection of p16 gene deletions in childhood acute lymphoblastic leukemia. Zuna J; Muzikova K; Hrusak O; Stary J; Trka J Haematologica; 2002 Jun; 87(6):668-9. PubMed ID: 12031930 [No Abstract] [Full Text] [Related]
16. Spiking of contemporary human template DNA with ancient DNA extracts induces mutations under PCR and generates nonauthentic mitochondrial sequences. Pusch CM; Bachmann L Mol Biol Evol; 2004 May; 21(5):957-64. PubMed ID: 15014140 [TBL] [Abstract][Full Text] [Related]
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18. EGFR sequence variations and real-time quantitative polymerase chain reaction analysis of gene dosage in brain metastases of solid tumors. Franco-Hernandez C; Martinez-Glez V; Arjona D; de Campos JM; Isla A; Gutierrez M; Vaquero J; Rey JA Cancer Genet Cytogenet; 2007 Feb; 173(1):63-7. PubMed ID: 17284372 [TBL] [Abstract][Full Text] [Related]
20. [The mitochondrial DNA mutation in spinocerebellar ataxia type 3]. Wang J; Luo M; Yuan Z; Yang X; Li G Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Dec; 25(6):667-9. PubMed ID: 19065528 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]