Y. Raashid

发表

Genotype-phenotype correlation for leber congenital amaurosis in Northern Pakistan.

K. Springell, M. Mohamed, M. McKibbin, 2010, Archives of ophthalmology.

Iatrogenic vesicovaginal fistula.

Y. Raashid, Tayyaba Tmajeed, Naeem Majeed, 2010, Journal of the College of Physicians and Surgeons--Pakistan : JCPSP.

Prenatal diagnosis of haemophilia-A: a basis for the Pakistani families.

T. Jameel, M. Anwar, M. Saleem, 1999, JPMA. The Journal of the Pakistan Medical Association.

Null mutations in LTBP2 cause primary congenital glaucoma.

D. Mackey, Shaheen N. Khan, S. Riazuddin, 2009, American journal of human genetics.

Prenatal diagnosis of beta‐thalassaemia in Pakistan: experience in a Muslim country

M. Petrou, B. Modell, M. Anwar, 2000, Prenatal diagnosis.

Refinement of the locus for hereditary congenital facial palsy on chromosome 3q21 in two unrelated families and screening of positional candidate genes

H. Brunner, H. Bokhoven, A. Brady, 2006, European Journal of Human Genetics.

Intrauterine Fetal Blood Transfusion (IUBT) for Rh Incompatibility - 12 Years' Experience from Pakistan.

G. Mason, H. Jafri, Y. Raashid, 2020, Journal of the College of Physicians and Surgeons--Pakistan : JCPSP.

Genetic heterogeneity for recessively inherited congenital cataract microcornea with corneal opacity.

Colin A. Johnson, A. Markham, M. Mohamed, 2011, Investigative ophthalmology & visual science.

Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma

M. McKibbin, C. Inglehearn, N. Fernandez-Fuentes, 2010, Molecular vision.

Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects

Colin A. Johnson, G. Taylor, M. Mohamed, 2011, Human molecular genetics.

An SCN9A channelopathy causes congenital inability to experience pain

Hussain Jafri, Emma Roberts, Enza Maria Valente, 2006, Nature.

Islam and termination of pregnancy for genetic conditions in Pakistan: implications for Pakistani health care providers

J. Hewison, H. Jafri, Y. Raashid, 2012, Prenatal diagnosis.

'All is done by Allah'. Understandings of Down syndrome and prenatal testing in Pakistan.

Hussain Jafri, Mushtaq Ahmed, H. Jafri, 2011, Social science & medicine.

Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma.

Colin A. Johnson, G. Taylor, J. Craig, 2011, American journal of human genetics.

A case for comprehensive antenatal screening for blood group antibodies.

Nadir Ali, M. F. Khattak, Y. Raashid, 1999, JPMA. The Journal of the Pakistan Medical Association.

Mpdz null allele in an avian model of retinal degeneration and mutations in human leber congenital amaurosis and retinitis pigmentosa.

S. Jacobson, D. Burt, K. Prescott, 2011, Investigative ophthalmology & visual science.

Founder mutations and genotype-phenotype correlations in Meckel-Gruber syndrome and associated ciliopathies

Colin A. Johnson, C. Logan, H. Lindsay, 2012, Cilia.

Pakistani mothers’ and fathers’ experiences and understandings of the diagnosis of Down syndrome for their child

H. Jafri, Y. Raashid, K. Ahmed, 2014, Journal of Community Genetics.

Experiences of parents with a child with Down syndrome in Pakistan and their views on termination of pregnancy

H. Jafri, Y. Raashid, L. Bryant, 2012, Journal of Community Genetics.

Umbilical vein oxytocin for the treatment of retained placenta (Release Study): a double-blind, randomised controlled trial

Z. Alfirevic, A. Weeks, G. Carroli, 2010, The Lancet.

Pakistani mothers’ and fathers’ experiences and understandings of the diagnosis of Down syndrome for their child

H. Jafri, Y. Raashid, K. Ahmed, 2014, Journal of Community Genetics.