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Muhammad Ansar

Showing results (61-70 of 191) with videos related to

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American Journal of Medical Genetics. Part A|January 17, 2012
Novel CLDN14 mutations in Pakistani families with autosomal recessive non-syndromic hearing lossKwanghyuk Lee, Muhammad Ansar, Paula B Andrade, et al.
Frontiers in Pediatrics|January 31, 2020
A Novel Homozygous Nonsense Mutation p.Cys366* in the WNT10B Gene Underlying Split-Hand/Split Foot Malformation in a Consanguineous Pakistani FamilyAmjad Khan, Rongrong Wang, Shirui Han, et al.
Iranian Journal of Basic Medical Sciences|September 23, 2020
Naphthoquinones from <i>Handroanthus impetiginosus</i> promote skin wound healing through Sirt3 regulationFayyaz Ahmad, Shaheen Bibi, Mincheol Kang, et al.
Journal of Medical Genetics|December 15, 2016
Recessive progressive symmetric erythrokeratoderma results from a homozygous loss-of-function mutation of <i>KRT83</i> and is allelic with dominant monilethrixKhadim Shah, Muhammad Ansar, Zaib-Un-Nisa Mughal, et al.
European Journal of Human Genetics : EJHG|September 27, 2003
DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22-q21.12Muhammad Wajid, Amir Ali Abbasi, Muhammad Ansar, et al.
Human Genomics|July 17, 2016
Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigreePeriklis Makrythanasis, Michel Guipponi, Federico A Santoni, et al.
Ophthalmic Research|November 15, 2021
Genetic Analysis of Consanguineous Pakistani Families with Congenital Stationary Night BlindnessHafiz Muhammad Azhar Baig, Muhammad Ansar, Afia Iqbal, et al.
Human Heredity|August 2, 2003
Localization of a novel autosomal recessive non-syndromic hearing impairment locus (DFNB38) to 6q26-q27 in a consanguineous kindred from PakistanMuhammad Ansar, Mohammad Ramzan, Thanh L Pham, et al.
The Science of the Total Environment|February 25, 2023
Antibiotics induced changes in nitrogen metabolism and antioxidative enzymes in mung bean (Vigna radiata)Marium Fiaz, Iftikhar Ahmed, Sumara Masood Ul Hassan, et al.
BMC Medical Genomics|August 28, 2021
Exome sequencing identifies novel and known mutations in families with intellectual disabilityMemoona Rasheed, Valeed Khan, Ricardo Harripaul, et al.
Pageof 20

Showing results (61-70 of 191) with videos related to

Sort By:
Pageof 20
American Journal of Medical Genetics. Part A|January 17, 2012
Novel CLDN14 mutations in Pakistani families with autosomal recessive non-syndromic hearing lossKwanghyuk Lee, Muhammad Ansar, Paula B Andrade, et al.
Frontiers in Pediatrics|January 31, 2020
A Novel Homozygous Nonsense Mutation p.Cys366* in the WNT10B Gene Underlying Split-Hand/Split Foot Malformation in a Consanguineous Pakistani FamilyAmjad Khan, Rongrong Wang, Shirui Han, et al.
Iranian Journal of Basic Medical Sciences|September 23, 2020
Naphthoquinones from <i>Handroanthus impetiginosus</i> promote skin wound healing through Sirt3 regulationFayyaz Ahmad, Shaheen Bibi, Mincheol Kang, et al.
Journal of Medical Genetics|December 15, 2016
Recessive progressive symmetric erythrokeratoderma results from a homozygous loss-of-function mutation of <i>KRT83</i> and is allelic with dominant monilethrixKhadim Shah, Muhammad Ansar, Zaib-Un-Nisa Mughal, et al.
European Journal of Human Genetics : EJHG|September 27, 2003
DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22-q21.12Muhammad Wajid, Amir Ali Abbasi, Muhammad Ansar, et al.
Human Genomics|July 17, 2016
Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigreePeriklis Makrythanasis, Michel Guipponi, Federico A Santoni, et al.
Ophthalmic Research|November 15, 2021
Genetic Analysis of Consanguineous Pakistani Families with Congenital Stationary Night BlindnessHafiz Muhammad Azhar Baig, Muhammad Ansar, Afia Iqbal, et al.
Human Heredity|August 2, 2003
Localization of a novel autosomal recessive non-syndromic hearing impairment locus (DFNB38) to 6q26-q27 in a consanguineous kindred from PakistanMuhammad Ansar, Mohammad Ramzan, Thanh L Pham, et al.
The Science of the Total Environment|February 25, 2023
Antibiotics induced changes in nitrogen metabolism and antioxidative enzymes in mung bean (Vigna radiata)Marium Fiaz, Iftikhar Ahmed, Sumara Masood Ul Hassan, et al.
BMC Medical Genomics|August 28, 2021
Exome sequencing identifies novel and known mutations in families with intellectual disabilityMemoona Rasheed, Valeed Khan, Ricardo Harripaul, et al.
Pageof 20