Lench NJ - Search Results

1

A third novel locus for primary autosomal recessive microcephaly maps to chromosome 9q34.

Moynihan L, Jackson AP, Roberts E, Karbani G, Lewis I, Corry P, Turner G, Mueller RF, Lench NJ, Woods CG. Moynihan L, et al. Among authors: lench nj. Am J Hum Genet. 2000 Feb;66(2):724-7. doi: 10.1086/302777. Am J Hum Genet. 2000. PMID: 10677332 Free PMC article.

2

DFNB20: a novel locus for autosomal recessive, non-syndromal sensorineural hearing loss maps to chromosome 11q25-qter.

Moynihan L, Houseman M, Newton V, Mueller R, Lench N. Moynihan L, et al. Eur J Hum Genet. 1999 Feb-Mar;7(2):243-6. doi: 10.1038/sj.ejhg.5200269. Eur J Hum Genet. 1999. PMID: 10196710

3

A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.

Campbell DA, McHale DP, Brown KA, Moynihan LM, Houseman M, Karbani G, Parry G, Janjua AH, Newton V, al-Gazali L, Markham AF, Lench NJ, Mueller RF. Campbell DA, et al. Among authors: lench nj. J Med Genet. 1997 Dec;34(12):1015-7. doi: 10.1136/jmg.34.12.1015. J Med Genet. 1997. PMID: 9429146 Free PMC article.

4

A syndrome of severe mental retardation, spasticity, and tapetoretinal degeneration linked to chromosome 15q24.

Mitchell SJ, McHale DP, Campbell DA, Lench NJ, Mueller RF, Bundey SE, Markham AF. Mitchell SJ, et al. Among authors: lench nj. Am J Hum Genet. 1998 May;62(5):1070-6. doi: 10.1086/301821. Am J Hum Genet. 1998. PMID: 9545391 Free PMC article.

5

Autozygosity mapping, to chromosome 11q25, of a rare autosomal recessive syndrome causing histiocytosis, joint contractures, and sensorineural deafness.

Moynihan LM, Bundey SE, Heath D, Jones EL, McHale DP, Mueller RF, Markham AF, Lench NJ. Moynihan LM, et al. Among authors: lench nj. Am J Hum Genet. 1998 May;62(5):1123-8. doi: 10.1086/301824. Am J Hum Genet. 1998. PMID: 9545394 Free PMC article.

6

Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter.

Jackson AP, McHale DP, Campbell DA, Jafri H, Rashid Y, Mannan J, Karbani G, Corry P, Levene MI, Mueller RF, Markham AF, Lench NJ, Woods CG. Jackson AP, et al. Among authors: lench nj. Am J Hum Genet. 1998 Aug;63(2):541-6. doi: 10.1086/301966. Am J Hum Genet. 1998. PMID: 9683597 Free PMC article.

7

A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25.

McHale DP, Mitchell S, Bundey S, Moynihan L, Campbell DA, Woods CG, Lench NJ, Mueller RF, Markham AF. McHale DP, et al. Among authors: lench nj. Am J Hum Genet. 1999 Feb;64(2):526-32. doi: 10.1086/302237. Am J Hum Genet. 1999. PMID: 9973289 Free PMC article.

8

The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1-13.2.

Roberts E, Jackson AP, Carradice AC, Deeble VJ, Mannan J, Rashid Y, Jafri H, McHale DP, Markham AF, Lench NJ, Woods CG. Roberts E, et al. Among authors: lench nj. Eur J Hum Genet. 1999 Oct-Nov;7(7):815-20. doi: 10.1038/sj.ejhg.5200385. Eur J Hum Genet. 1999. PMID: 10573015

9

A gene for ataxic cerebral palsy maps to chromosome 9p12-q12.

McHale DP, Jackson AP, Campbell, Levene MI, Corry P, Woods CG, Lench NJ, Mueller RF, Markham AF. McHale DP, et al. Among authors: lench nj. Eur J Hum Genet. 2000 Apr;8(4):267-72. doi: 10.1038/sj.ejhg.5200445. Eur J Hum Genet. 2000. PMID: 10854109

10

Mapping of the DFNB1 locus.

Mueller RF, Lench NJ. Mueller RF, et al. Among authors: lench nj. Adv Otorhinolaryngol. 2000;56:116-23. doi: 10.1159/000059090. Adv Otorhinolaryngol. 2000. PMID: 10868223 Review. No abstract available.

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