Markham AF - Search Results

1

Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175.

Brown KA, Janjua AH, Karbani G, Parry G, Noble A, Crockford G, Bishop DT, Newton VE, Markham AF, Mueller RF. Brown KA, et al. Among authors: markham af. Hum Mol Genet. 1996 Jan;5(1):169-73. doi: 10.1093/hmg/5.1.169. Hum Mol Genet. 1996. PMID: 8789457

2

Human sequences homologous to the gene for the cochlear protein Ocp-II do not map to currently known non-syndromic hearing loss loci.

Brown KA, Leek JP, Lench NJ, Moynihan LM, Markham AF, Mueller RF. Brown KA, et al. Among authors: markham af. Ann Hum Genet. 1996 Sep;60(5):385-9. doi: 10.1111/j.1469-1809.1996.tb00436.x. Ann Hum Genet. 1996. PMID: 8912791

3

Genetic heterogeneity in Schwartz-Jampel syndrome: two families with neonatal Schwartz-Jampel syndrome do not map to human chromosome 1p34-p36.1.

Brown KA, al-Gazali LI, Moynihan LM, Lench NJ, Markham AF, Mueller RF. Brown KA, et al. Among authors: markham af. J Med Genet. 1997 Aug;34(8):685-7. doi: 10.1136/jmg.34.8.685. J Med Genet. 1997. PMID: 9279765 Free PMC article.

4

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: markham af. 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.

5

A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2).

Lench NJ, Markham AF, Mueller RF, Kelsell DP, Smith RJ, Willems PJ, Schatteman I, Capon H, Van De Heyning PJ, Van Camp G. Lench NJ, et al. Among authors: markham af. J Med Genet. 1998 Feb;35(2):151-2. doi: 10.1136/jmg.35.2.151. J Med Genet. 1998. PMID: 9507396 Free PMC article.

6

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: markham af. Am J Hum Genet. 1998 May;62(5):1123-8. doi: 10.1086/301824. Am J Hum Genet. 1998. PMID: 9545394 Free PMC article.

7

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: markham af. Am J Hum Genet. 1998 Aug;63(2):541-6. doi: 10.1086/301966. Am J Hum Genet. 1998. PMID: 9683597 Free PMC article.

8

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: markham af. Am J Hum Genet. 1999 Feb;64(2):526-32. doi: 10.1086/302237. Am J Hum Genet. 1999. PMID: 9973289 Free PMC article.

9

A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31.

Pulleyn LJ, Jackson AP, Roberts E, Carridice A, Muxworthy C, Houseman M, Al-Gazali LI, Lench NJ, Markham AF, Mueller RF. Pulleyn LJ, et al. Among authors: markham af. Eur J Hum Genet. 2000 Dec;8(12):991-3. doi: 10.1038/sj.ejhg.5200567. Eur J Hum Genet. 2000. PMID: 11175289

10

Identification of microcephalin, a protein implicated in determining the size of the human brain.

Jackson AP, Eastwood H, Bell SM, Adu J, Toomes C, Carr IM, Roberts E, Hampshire DJ, Crow YJ, Mighell AJ, Karbani G, Jafri H, Rashid Y, Mueller RF, Markham AF, Woods CG. Jackson AP, et al. Among authors: markham af. Am J Hum Genet. 2002 Jul;71(1):136-42. doi: 10.1086/341283. Epub 2002 Jun 3. Am J Hum Genet. 2002. PMID: 12046007 Free PMC article.

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