Mao JI - Search Results

1

A functional neo-centromere formed through activation of a latent human centromere and consisting of non-alpha-satellite DNA.

du Sart D, Cancilla MR, Earle E, Mao JI, Saffery R, Tainton KM, Kalitsis P, Martyn J, Barry AE, Choo KH. du Sart D, et al. Among authors: mao ji. Nat Genet. 1997 Jun;16(2):144-53. doi: 10.1038/ng0697-144. Nat Genet. 1997. PMID: 9171825

2

A common region of 10p deleted in DiGeorge and velocardiofacial syndromes.

Daw SC, Taylor C, Kraman M, Call K, Mao J, Schuffenhauer S, Meitinger T, Lipson T, Goodship J, Scambler P. Daw SC, et al. Nat Genet. 1996 Aug;13(4):458-60. doi: 10.1038/ng0896-458. Nat Genet. 1996. PMID: 8696341

3

Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2.

Jabs EW, Li X, Scott AF, Meyers G, Chen W, Eccles M, Mao JI, Charnas LR, Jackson CE, Jaye M. Jabs EW, et al. Among authors: mao ji. Nat Genet. 1994 Nov;8(3):275-9. doi: 10.1038/ng1194-275. Nat Genet. 1994. PMID: 7874170

4

FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis.

Hewett DR, Handt O, Hobson L, Mangelsdorf M, Eyre HJ, Baker E, Sutherland GR, Schuffenhauer S, Mao JI, Richards RI. Hewett DR, et al. Among authors: mao ji. Mol Cell. 1998 May;1(6):773-81. doi: 10.1016/s1097-2765(00)80077-5. Mol Cell. 1998. PMID: 9660961 Free article.

5

Positional cloning of a gene for Hermansky-Pudlak syndrome, a disorder of cytoplasmic organelles.

Oh J, Bailin T, Fukai K, Feng GH, Ho L, Mao JI, Frenk E, Tamura N, Spritz RA. Oh J, et al. Among authors: mao ji. Nat Genet. 1996 Nov;14(3):300-6. doi: 10.1038/ng1196-300. Nat Genet. 1996. PMID: 8896559

6

Physical and linkage mapping of human carbamyl phosphate synthetase I (CPS1) and reassignment from 2p to 2q35.

Summar ML, Dasouki MJ, Schofield PJ, Krishnamani MR, Vnencak-Jones C, Tuchman M, Mao J, Phillips JA 3rd. Summar ML, et al. Cytogenet Cell Genet. 1995;71(3):266-7. doi: 10.1159/000134124. Cytogenet Cell Genet. 1995. PMID: 7587391

7

Identification and molecular confirmation of a small chromosome 10q duplication [dir dup(10)(q24.2-->q24.3)] inherited from a mother mosaic for the abnormality.

Tonk V, Schneider NR, Delgado MR, Mao J, Schultz RA. Tonk V, et al. Am J Med Genet. 1996 Jan 2;61(1):16-20. doi: 10.1002/(SICI)1096-8628(19960102)61:1<16::AID-AJMG3>3.0.CO;2-V. Am J Med Genet. 1996. PMID: 8741911

8

Genetic mapping of the human growth hormone-releasing factor gene (GHRF) using two intragenic polymorphisms detected by PCR amplification.

Pérez Jurado LA, Phillips JA 3rd, Summar ML, Mao J, Weber JL, Schaefer FV, Hazan J, Argente J. Pérez Jurado LA, et al. Genomics. 1994 Mar 1;20(1):132-4. doi: 10.1006/geno.1994.1140. Genomics. 1994. PMID: 8020943

9

Paternal pericentric inversion of chromosome 4 as a cause of recurrent pregnancy loss.

Wolf GC, Mao J, Izquierdo L, Joffe G. Wolf GC, et al. J Med Genet. 1994 Feb;31(2):153-5. doi: 10.1136/jmg.31.2.153. J Med Genet. 1994. PMID: 8182725 Free PMC article.

10

A case report of neuralgic amyotrophy.

Sun J, Mao J, Zhang F, Gui X, Liao J. Sun J, et al. Among authors: mao j. Front Neurol. 2024 May 23;15:1392766. doi: 10.3389/fneur.2024.1392766. eCollection 2024. Front Neurol. 2024. PMID: 38846034 Free PMC article.

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