Batch JA - Search Results

1

Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome.

Batch JA, Williams DM, Davies HR, Brown BD, Evans BA, Hughes IA, Patterson MN. Batch JA, et al. Hum Mol Genet. 1992 Oct;1(7):497-503. doi: 10.1093/hmg/1.7.497. Hum Mol Genet. 1992. PMID: 1307250

2

Male pseudohermaphroditism: clinical management, diagnosis and treatment.

Hughes IA, Williams DM, Batch JA, Patterson MN. Hughes IA, et al. Among authors: batch ja. Horm Res. 1992;38 Suppl 2:77-81. doi: 10.1159/000182604. Horm Res. 1992. PMID: 1292987 Review.

3

Role of the androgen receptor in male sexual differentiation.

Batch JA, Williams DM, Davies HR, Brown BD, Evans BA, Hughes IA, Patterson MN. Batch JA, et al. Horm Res. 1992;38(5-6):226-9. doi: 10.1159/000182548. Horm Res. 1992. PMID: 1307741

4

Mutations of the androgen receptor gene identified in perineal hypospadias.

Batch JA, Evans BA, Hughes IA, Patterson MN. Batch JA, et al. J Med Genet. 1993 Mar;30(3):198-201. doi: 10.1136/jmg.30.3.198. J Med Genet. 1993. PMID: 8097257 Free PMC article.

5

Phenotypic variation and detection of carrier status in the partial androgen insensitivity syndrome.

Batch JA, Davies HR, Evans BA, Hughes IA, Patterson MN. Batch JA, et al. Arch Dis Child. 1993 Apr;68(4):453-7. doi: 10.1136/adc.68.4.453. Arch Dis Child. 1993. PMID: 8099270 Free PMC article.

6

Prevalence of mutations in the short stature homeobox containing gene (SHOX) in Madelung deformity of childhood.

Flanagan SF, Munns CF, Hayes M, Williams B, Berry M, Vickers D, Rao E, Rappold GA, Batch JA, Hyland VJ, Glass IA. Flanagan SF, et al. Among authors: batch ja. J Med Genet. 2002 Oct;39(10):758-63. doi: 10.1136/jmg.39.10.758. J Med Genet. 2002. PMID: 12362035 Free PMC article. No abstract available.

7

Expression of SHOX in human fetal and childhood growth plate.

Munns CJ, Haase HR, Crowther LM, Hayes MT, Blaschke R, Rappold G, Glass IA, Batch JA. Munns CJ, et al. Among authors: batch ja. J Clin Endocrinol Metab. 2004 Aug;89(8):4130-5. doi: 10.1210/jc.2003-032230. J Clin Endocrinol Metab. 2004. PMID: 15292358

8

Trisomy of the short stature homeobox-containing gene (SHOX), resulting from a duplication-deletion of the X chromosome.

Adamson KA, Cross I, Batch JA, Rappold GA, Glass IA, Ball SG. Adamson KA, et al. Among authors: batch ja. Clin Endocrinol (Oxf). 2002 May;56(5):671-5. doi: 10.1046/j.1365-2265.2002.01504.x. Clin Endocrinol (Oxf). 2002. PMID: 12035792

9

Familial growth and skeletal features associated with SHOX haploinsufficiency.

Munns CF, Glass IA, Flanagan S, Hayes M, Williams B, Berry M, Vickers D, O'Rourke P, Rao E, Rappold GA, Hyland VJ, Batch JA. Munns CF, et al. Among authors: batch ja. J Pediatr Endocrinol Metab. 2003 Sep;16(7):987-96. doi: 10.1515/jpem.2003.16.7.987. J Pediatr Endocrinol Metab. 2003. PMID: 14513875

10

Effect of 24 months of recombinant growth hormone on height and body proportions in SHOX haploinsufficiency.

Munns CF, Berry M, Vickers D, Rappold GA, Hyland VJ, Glass IA, Batch JA. Munns CF, et al. Among authors: batch ja. J Pediatr Endocrinol Metab. 2003 Sep;16(7):997-1004. doi: 10.1515/jpem.2003.16.7.997. J Pediatr Endocrinol Metab. 2003. PMID: 14513876 Clinical Trial.

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