Metabolic markers in male infertility: a pilot study von Kajal Sihag, Ashutosh Halder, Mona Sharma

Volltext

Serum anti-Müllerian hormone: A potential biomarker for polycystic ovary syndrome von Halder, Ashutosh, Kumar, Hemant, Sharma, Mona, Jain, Manish, Kalsi, Amanpreet Kaur, Pandey, Shivam

Volltext

An investigation of steroid biosynthesis pathway genes in women with polycystic ovary syndrome von Sharma, Priyal, Jain, Manish, Halder, Ashutosh

Volltext

Human reproductive genetics: Emerging technologies & clinical applications von Halder, Ashutosh

Volltext

22(R)-hydroxycholesterol for dopaminergic neuronal specification of MSCs and amelioration of Parkinsonian symptoms in rats von Singh, Manisha, Jain, Manish, Bose, Samrat, Halder, Ashutosh, Nag, Tapas Chandra, Dinda, Amit Kumar, Mohanty, Sujata

Volltext

Dihydrotestosterone- A Potential Biomarker of Hyperandrogenaemia in Polycystic Ovary Syndrome: A Case-control Study from North India von Kumar, Hemant, Halder, Ashutosh, Sharma, Mona, Jain, Manish, Kalsi, Amanpreet Kaur

Volltext

Association of Cadmium, Chromium, Manganese and Lead with Hyperprolactinemia: A Pilot Study von Kalsi, Amanpreet Kaur, Halder, Ashutosh, Jain, Manish, Srivastava, Amita

Volltext

The therapeutic effect of bone marrow–derived liver cells in the phenotypic correction of murine hemophilia A von Yadav, Neelam, Kanjirakkuzhiyil, Sumod, Kumar, Suresh, Jain, Manish, Halder, Ashutosh, Saxena, Renu, Mukhopadhyay, Asok

Volltext

Chromosome 22q11.2 microdeletion in monozygotic twins with discordant phenotype and deletion size von Halder, Ashutosh, Jain, Manish, Chaudhary, Isha, Varma, Binuja

Volltext

CFTR gene variants in Indian congenital bilateral absence of vas deferens & its relevance in genetic counselling von Halder, Ashutosh, Pandey, Deepak

Volltext

SNP Microarray in FISH Negative Clinically Suspected 22q11.2 Microdeletion Syndrome von Halder, Ashutosh, Kalsi, Amanpreet Kaur, Jain, Manish

Volltext

Cytokine profile in multiple myeloma von Jasrotia, Shivali, Gupta, Ritu, Sharma, Atul, Halder, Ashutosh, Kumar, Lalit

Volltext

Prevalence of 22q11.2 microdeletion in 146 patients with cardiac malformation in a referral hospital of North India von Halder, Ashutosh, Jain, Manish, Chaudhary, Isha, Kabra, Madhulika

Volltext

The Sertoli Cell Only Syndrome and Glaucoma in a Sex - Determining Region Y (SRY) Positive XX Infertile Male von Jain, Manish, V, Veeramohan, Chaudhary, Isha, Halder, Ashutosh

Volltext

Identification of genomic imbalances (CNVs as well as LOH) in sertoli cell only syndrome cases through cytoscan microarray von Sharma, Aiyush, Jain, Manish, Halder, Ashutosh, Kaushal, Seema

Volltext

Mosaic 22q11.2 microdeletion syndrome: diagnosis and clinical manifestations of two cases von Halder, Ashutosh, Jain, Manish, Kabra, Madhulika, Gupta, Neerja

Volltext

Placental chimerism in early human pregnancy von Ashutosh, Halder

Volltext

Male-like external genitalia with epididymis in a case of 46, XX disorder of sex development due to congenital adrenal hyperplasia von Ashutosh Halder, Ramesh Kumar Gupta

Volltext

Prevalence and reproductive manifestations of macroprolactinemia von Kalsi, Amanpreet Kaur, Halder, Ashutosh, Jain, Manish, Chaturvedi, P. K., Sharma, J. B.

Volltext

Lethal Developmental Defects: An Overview von Halder, Ashutosh

Volltext