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The Journal of Steroid Biochemistry and Molecular Biology
|
December 1, 1992
Prenatal prediction of androgen insensitivity syndrome using exon 1 polymorphism of the androgen receptor gene
J M Lobaccaro, S Lumbroso, F C Pigeon, et al.
Clinical Endocrinology
|
March 1, 1994
Molecular prenatal diagnosis of partial androgen insensitivity syndrome based on the Hind III polymorphism of the androgen receptor gene
J M Lobaccaro, C Belon, S Lumbroso, et al.
Journal of Medical Genetics
|
May 12, 2009
Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2
P Laissue, B Lakhal, B A Benayoun, et al.
Human Reproduction (Oxford, England)
|
May 30, 2008
A new LH receptor splice mutation responsible for male hypogonadism with subnormal sperm production in the propositus, and infertility with regular cycles in an affected sister
M Bruysters, S Christin-Maitre, M Verhoef-Post, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
May 15, 2002
Mutations of the 5alpha-steroid reductase type 2 gene in six Turkish patients from unrelated families and a large pedigree of an isolated Turkish village
G Ocal, P Adiyaman, M Berberoğlu, et al.
Annales D'Endocrinologie
|
May 9, 2008
[Complete androgen insensitivity syndrome: a novel mutation in a Tunisian family]
D Bel Hadj Youssef, M Kacem, I Khochtali, et al.
Clinical Genetics
|
December 30, 2016
SF1 and spleen development: new heterozygous mutation, literature review and consequences for NR5A1-mutated patient's management
C Colson, E Aubry, M Cartigny, et al.
Neurology International
|
December 27, 2024
Mechanisms of Neurosyphilis-Induced Dementia: Insights into Pathophysiology
Aya Fadel, Hussain Hussain, Robert J Hernandez, et al.
Human Mutation
|
March 27, 1999
The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor
A S Barbosa, C G Hadjiathanasiou, C Theodoridis, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 1, 2005
A nationwide study of granulosa cell tumors in pre- and postpubertal girls: missed diagnosis of endocrine manifestations worsens prognosis
N Kalfa, C Patte, D Orbach, et al.
Page
of 29
Search research articles
Search
Showing results (271-280 of 284) with videos related to
Sort By:
Page
of 29
The Journal of Steroid Biochemistry and Molecular Biology
|
December 1, 1992
Prenatal prediction of androgen insensitivity syndrome using exon 1 polymorphism of the androgen receptor gene
J M Lobaccaro, S Lumbroso, F C Pigeon, et al.
Clinical Endocrinology
|
March 1, 1994
Molecular prenatal diagnosis of partial androgen insensitivity syndrome based on the Hind III polymorphism of the androgen receptor gene
J M Lobaccaro, C Belon, S Lumbroso, et al.
Journal of Medical Genetics
|
May 12, 2009
Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2
P Laissue, B Lakhal, B A Benayoun, et al.
Human Reproduction (Oxford, England)
|
May 30, 2008
A new LH receptor splice mutation responsible for male hypogonadism with subnormal sperm production in the propositus, and infertility with regular cycles in an affected sister
M Bruysters, S Christin-Maitre, M Verhoef-Post, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
May 15, 2002
Mutations of the 5alpha-steroid reductase type 2 gene in six Turkish patients from unrelated families and a large pedigree of an isolated Turkish village
G Ocal, P Adiyaman, M Berberoğlu, et al.
Annales D'Endocrinologie
|
May 9, 2008
[Complete androgen insensitivity syndrome: a novel mutation in a Tunisian family]
D Bel Hadj Youssef, M Kacem, I Khochtali, et al.
Clinical Genetics
|
December 30, 2016
SF1 and spleen development: new heterozygous mutation, literature review and consequences for NR5A1-mutated patient's management
C Colson, E Aubry, M Cartigny, et al.
Neurology International
|
December 27, 2024
Mechanisms of Neurosyphilis-Induced Dementia: Insights into Pathophysiology
Aya Fadel, Hussain Hussain, Robert J Hernandez, et al.
Human Mutation
|
March 27, 1999
The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor
A S Barbosa, C G Hadjiathanasiou, C Theodoridis, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 1, 2005
A nationwide study of granulosa cell tumors in pre- and postpubertal girls: missed diagnosis of endocrine manifestations worsens prognosis
N Kalfa, C Patte, D Orbach, et al.
Page
of 29