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The Indian Journal of Medical Research
|
February 4, 2006
A preliminary investigation of genomic screening in cervical carcinoma by comparative genomic hybridization
Ashutosh Halder, Shikha Halder, Ashish Fauzdar
Scientifica
|
April 7, 2016
SNP Microarray in FISH Negative Clinically Suspected 22q11.2 Microdeletion Syndrome
Ashutosh Halder, Manish Jain, Amanpreet Kaur Kalsi
Molecular Cytogenetics
|
August 12, 2008
Mosaic 22q11.2 microdeletion syndrome: diagnosis and clinical manifestations of two cases
Ashutosh Halder, Manish Jain, Madhulika Kabra, et al.
Molecular Cytogenetics
|
March 15, 2012
Chromosome 22q11.2 microdeletion in monozygotic twins with discordant phenotype and deletion size
Ashutosh Halder, Manish Jain, Isha Chaudhary, et al.
Gene
|
July 18, 2021
Identification of genomic imbalances (CNVs as well as LOH) in sertoli cell only syndrome cases through cytoscan microarray
Aiyush Sharma, Manish Jain, Ashutosh Halder, et al.
Asian Journal of Andrology
|
June 5, 2003
Absence of sperm meiotic segregation error of chromosomes 1, 9, 12, 13, 16, 18, 21, X and Y in a case of 100% necrozoospermia
Ashutosh Halder, Vandana Chaddha, Savita Agarwal, et al.
Journal of Clinical and Diagnostic Research : JCDR
|
September 3, 2013
The Sertoli Cell Only Syndrome and Glaucoma in a Sex - Determining Region Y (SRY) Positive XX Infertile Male
Manish Jain, Veeramohan V, Isha Chaudhary, et al.
Journal of Human Reproductive Sciences
|
February 7, 2024
Whole Exome Sequencing Reveals Rare Variants in Genes Associated with Metabolic Disorders in Women with PCOS
Priyal Sharma, Ashutosh Halder, Manish Jain, et al.
Reproductive Biology
|
May 28, 2021
Sex ratio trajectory in mouse
Ashutosh Halder, Isha Chaudhary, Manish Jain, et al.
Indian Pediatrics
|
January 21, 2006
Detection of 22 q11.2 hemizygous deletion by interphase FISH in a patient with features of CATCH 22 syndrome
Ashutosh Halder, Ashish Fauzdar, Madhulika Kabra, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 44) with videos related to
Sort By:
Page
of 5
The Indian Journal of Medical Research
|
February 4, 2006
A preliminary investigation of genomic screening in cervical carcinoma by comparative genomic hybridization
Ashutosh Halder, Shikha Halder, Ashish Fauzdar
Scientifica
|
April 7, 2016
SNP Microarray in FISH Negative Clinically Suspected 22q11.2 Microdeletion Syndrome
Ashutosh Halder, Manish Jain, Amanpreet Kaur Kalsi
Molecular Cytogenetics
|
August 12, 2008
Mosaic 22q11.2 microdeletion syndrome: diagnosis and clinical manifestations of two cases
Ashutosh Halder, Manish Jain, Madhulika Kabra, et al.
Molecular Cytogenetics
|
March 15, 2012
Chromosome 22q11.2 microdeletion in monozygotic twins with discordant phenotype and deletion size
Ashutosh Halder, Manish Jain, Isha Chaudhary, et al.
Gene
|
July 18, 2021
Identification of genomic imbalances (CNVs as well as LOH) in sertoli cell only syndrome cases through cytoscan microarray
Aiyush Sharma, Manish Jain, Ashutosh Halder, et al.
Asian Journal of Andrology
|
June 5, 2003
Absence of sperm meiotic segregation error of chromosomes 1, 9, 12, 13, 16, 18, 21, X and Y in a case of 100% necrozoospermia
Ashutosh Halder, Vandana Chaddha, Savita Agarwal, et al.
Journal of Clinical and Diagnostic Research : JCDR
|
September 3, 2013
The Sertoli Cell Only Syndrome and Glaucoma in a Sex - Determining Region Y (SRY) Positive XX Infertile Male
Manish Jain, Veeramohan V, Isha Chaudhary, et al.
Journal of Human Reproductive Sciences
|
February 7, 2024
Whole Exome Sequencing Reveals Rare Variants in Genes Associated with Metabolic Disorders in Women with PCOS
Priyal Sharma, Ashutosh Halder, Manish Jain, et al.
Reproductive Biology
|
May 28, 2021
Sex ratio trajectory in mouse
Ashutosh Halder, Isha Chaudhary, Manish Jain, et al.
Indian Pediatrics
|
January 21, 2006
Detection of 22 q11.2 hemizygous deletion by interphase FISH in a patient with features of CATCH 22 syndrome
Ashutosh Halder, Ashish Fauzdar, Madhulika Kabra, et al.
Page
of 5