X. Zhao

Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting

T. Beaty, D. Cutler, Xuefang Zhao, 2022, medRxiv.

Gene analysis and prenatal diagnosis for two families of congenital factor V deficiency

Z. Wang, C. Ruan, J. Ding, 2011, Haemophilia : the official journal of the World Federation of Hemophilia.

In a shake of a lamb's tail: using genomics to unravel a cause of chondrodysplasia in Texel sheep.

M. Rothschild, S. Onteru, H. Blair, 2012, Animal genetics.

A genome-wide association study for canine cryptorchidism in Siberian Huskies.

M. Rothschild, S. Onteru, M. Saatchi, 2014, Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie.

An association study of 20 candidate genes with cryptorchidism in Siberian Husky dogs.

M. Rothschild, Z. Du, X. Zhao, 2010, Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie.

Spastic paraplegia, ataxia, mental retardation (SPAR): A novel genetic disorder

K. Lindblad, P. Hedera, M. Schalling, 2002, Neurology.

Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q.

M. Leppert, P. Hedera, J. Fink, 1999, American journal of human genetics.

A genome-wide association study for canine cryptorchidism in Siberian

M. Rothschild, S. Onteru, M. Saatchi, 2014 .

A missense mutation in AGTPBP1 was identified in sheep with a lower motor neuron disease

M. Rothschild, S. Onteru, H. Blair, 2012, Heredity.

[Clinical phenotype and gene analysis of 86 cases of 5 alpha reductase deficiency].

C. Gong, X. Zhao, L. Fan, 2019, Zhonghua er ke za zhi = Chinese journal of pediatrics.