Milner RD - Search Results

1

Genetic mapping of the FACC gene and linkage analysis in Fanconi anaemia families.

Gibson RA, Ford D, Jansen S, Savoia A, Havenga C, Milner RD, de Ravel TJ, Cohn RJ, Ball SE, Roberts I, et al. Gibson RA, et al. Among authors: milner rd. J Med Genet. 1994 Nov;31(11):868-71. doi: 10.1136/jmg.31.11.868. J Med Genet. 1994. PMID: 7853372 Free PMC article.

2

Novel mutations and polymorphisms in the Fanconi anemia group C gene.

Gibson RA, Morgan NV, Goldstein LH, Pearson IC, Kesterton IP, Foot NJ, Jansen S, Havenga C, Pearson T, de Ravel TJ, Cohn RJ, Marques IM, Dokal I, Roberts I, Marsh J, Ball S, Milner RD, Llerena JC Jr, Samochatova E, Mohan SP, Vasudevan P, Birjandi F, Hajianpour A, Murer-Orlando M, Mathew CG. Gibson RA, et al. Among authors: milner rd. Hum Mutat. 1996;8(2):140-8. doi: 10.1002/(SICI)1098-1004(1996)8:2<140::AID-HUMU6>3.0.CO;2-F. Hum Mutat. 1996. PMID: 8844212

3

A new autosomal recessive anomaly mimicking Fanconi's anaemia phenotype.

Milner RD, Khallouf KA, Gibson R, Hajianpour A, Mathew CG. Milner RD, et al. Arch Dis Child. 1993 Jan;68(1):101-3. doi: 10.1136/adc.68.1.101. Arch Dis Child. 1993. PMID: 8434992 Free PMC article.

4

Genetic linkage studies of X-linked hypophosphataemic rickets in a Saudi Arabian family.

Thakker RV, Farmery MR, Sakati NA, Milner RD. Thakker RV, et al. Among authors: milner rd. Clin Endocrinol (Oxf). 1992 Oct;37(4):338-43. doi: 10.1111/j.1365-2265.1992.tb02335.x. Clin Endocrinol (Oxf). 1992. PMID: 1483289

5

Familial growth hormone deficiency: a model of dominant and recessive mutations affecting a monomeric protein.

Cogan JD, Phillips JA 3rd, Schenkman SS, Milner RD, Sakati N. Cogan JD, et al. Among authors: milner rd. J Clin Endocrinol Metab. 1994 Nov;79(5):1261-5. doi: 10.1210/jcem.79.5.7962317. J Clin Endocrinol Metab. 1994. PMID: 7962317

6

Heterogeneous growth hormone (GH) gene mutations in familial GH deficiency.

Cogan JD, Phillips JA 3rd, Sakati N, Frisch H, Schober E, Milner RD. Cogan JD, et al. Among authors: milner rd. J Clin Endocrinol Metab. 1993 May;76(5):1224-8. doi: 10.1210/jcem.76.5.8496314. J Clin Endocrinol Metab. 1993. PMID: 8496314

7

A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features.

Sanjad SA, Sakati NA, Abu-Osba YK, Kaddoura R, Milner RD. Sanjad SA, et al. Among authors: milner rd. Arch Dis Child. 1991 Feb;66(2):193-6. doi: 10.1136/adc.66.2.193. Arch Dis Child. 1991. PMID: 2001103 Free PMC article.

8

Pro239Ser: a novel recessive mutation of the Pit-1 gene in seven Middle Eastern children with growth hormone, prolactin, and thyrotropin deficiency.

Pernasetti F, Milner RD, al Ashwal AA, de Zegher F, Chavez VM, Muller M, Martial JA. Pernasetti F, et al. Among authors: milner rd. J Clin Endocrinol Metab. 1998 Jun;83(6):2079-83. doi: 10.1210/jcem.83.6.4901. J Clin Endocrinol Metab. 1998. PMID: 9626142 Free article.

9

Growth failure secondary to moyamoya syndrome.

MacKenzie CA, Milner RD, Bergvall U, Powell T. MacKenzie CA, et al. Among authors: milner rd. Arch Dis Child. 1990 Feb;65(2):232-3. doi: 10.1136/adc.65.2.232. Arch Dis Child. 1990. PMID: 2317074 Free PMC article.

10

Changes in leg length and height during treatment with somatotropin.

Wales JK, Milner RD. Wales JK, et al. Among authors: milner rd. Arch Dis Child. 1989 Dec;64(12):1708-12. doi: 10.1136/adc.64.12.1708. Arch Dis Child. 1989. PMID: 2696434 Free PMC article. Clinical Trial.

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