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24 in total

1. Biochemical and DNA markers of X-linked hypophosphataemic rickets: a study of sporadic cases.

Authors: E Pronicka; E Popowska; E Rowińska; D Piekutowska; M Oglecka; M Krajewska-Walasek
Journal: J Inherit Metab Dis Date: 1992 Impact factor: 4.982

2. Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase.

Authors: J B Bateman
Journal: Trans Am Ophthalmol Soc Date: 1992

3. Hypohidrotic Ectodermal Dysplasia.

Authors: Gaurav Pratap Singh; Vivek Saxena
Journal: Med J Armed Forces India Date: 2014-08-05

4. Current position of paternity tests.

Authors:
Journal: Br Med J Date: 1977-07-16

5. X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis.

Authors: J Zonana; A Clarke; M Sarfarazi; N S Thomas; K Roberts; K Marymee; P S Harper
Journal: Am J Hum Genet Date: 1988-07 Impact factor: 11.025

6. Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome).

Authors: K D MacDermot; R M Winter; S Malcolm
Journal: Hum Genet Date: 1986-10 Impact factor: 4.132

7. Comparison of point mutation rates in different species with human mutation rates.

Authors: P Propping
Journal: Humangenetik Date: 1972

8. "Private" genetic variants and the frequency of mutation among South American Indians.

Authors: J V Neel
Journal: Proc Natl Acad Sci U S A Date: 1973-12 Impact factor: 11.205

9. Why must drugs and other environmental agents be tested for mutagenicity.

Authors: F Vogel
Journal: Arch Toxikol Date: 1971

10. Ectodermal dysplasia - Maxillary and mandibular alveolar reconstruction with dental rehabilitation: A case report and review of the literature.

Authors: Sanjeev N Deshpande; Vikas Kumar
Journal: Indian J Plast Surg Date: 2010-01