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Ki-67 detects a nuclear matrix-associated proliferation-related antigen. I: Intracellular localization during interphase

Journal of cell science, 1989, Vol.92 (1), p.123-130

1989

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Androgen insensitivity syndrome (AIS): emotional reactions of parents and adult patients to the clinical diagnosis of AIS and its confirmation by androgen receptor gene mutation analysis

Hormone research, 2000, Vol.53 (1), p.9-15

2000

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Molecular Analysis of the Androgen-Receptor Gene in a Family with Receptor-Positive Partial Androgen Insensitivity: An Unusual Type of Intronic Mutation

American journal of human genetics, 1997-11, Vol.61 (5), p.1067-1077

1997

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Germ-line and somatic mosaicism in the androgen insensitivity syndrome : Implications for genetic counseling

American journal of human genetics, 1997-04, Vol.60 (4), p.1003-1006

1997

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Androgen receptor mutations

Journal of steroid biochemistry and molecular biology, 1995-06, Vol.53 (1), p.443-448

1995

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Genotype versus phenotype in families with androgen insensitivity syndrome

The journal of clinical endocrinology and metabolism, 2001-09, Vol.86 (9), p.4151-4160

2001

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Molecular basis of androgen insensitivity

The Journal of steroid biochemistry and molecular biology, 1996-08, Vol.58 (5), p.569-575

1996

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17β-Hydroxysteroid dehydrogenase-3 deficiency: Diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de Novo mutations

The journal of clinical endocrinology and metabolism, 1999, Vol.84 (12), p.4713-4721

1999

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Phenotypic Variation in a Family with Partial Androgen Insensitivity Syndrome Explained by Differences in 5 Dihydrotestosterone Availability

The journal of clinical endocrinology and metabolism, 2001-03, Vol.86 (3), p.1240-1246

Boehmer, A. L. M.

2001

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17 -Hydroxysteroid Dehydrogenase-3 Deficiency: Diagnosis, Phenotypic Variability, Population Genetics, and Worldwide Distribution of Ancient and de Novo Mutations

The journal of clinical endocrinology and metabolism, 1999-12, Vol.84 (12), p.4713-4721

Boehmer, A. L. M.

1999

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ETIOLOGICAL STUDIES OF SEVERE OR FAMILIAL HYPOSPADIAS

The Journal of urology, 2001-04, Vol.165 (4), p.1246-1254

2001

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Androgens and fetal growth

Hormone research, 1998, Vol.50 (4), p.243-244

1998

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Moeilijk behandelbaar astma: diagnostiek en behandelopties

Tijdschrift voor kindergeneeskunde, 2009, Vol.77 (6), p.255-262

2009

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Phenotypic variation in a family with partial androgen insensitivity syndrome explained by differences in 5alpha dihydrotestosterone availability

The journal of clinical endocrinology and metabolism, 2001-03, Vol.86 (3), p.1240-1246

2001

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From gene to disease; androgen receptor gene, androgen insensitivity syndrome, and spinal and bulbar muscle atrophy

Nederlands tijdschrift voor geneeskunde, 2001-12, Vol.145 (48), p.2326

2001

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Substitution of Ala564 in the first zinc cluster of the deoxyribonucleic acid (DNA)-binding domain of the androgen receptor by Asp, Asn, or Leu exerts differential effects on DNA binding

Endocrinology (Philadelphia), 1998-01, Vol.139 (1), p.103-110

1998

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MITTELRÄTIEN

Verzeichniss Rätoromanischer Litteratur, 2021, Vol.20 (6, 2), p.205-211

Boehmer, Ed

2021

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GRAUBÜNDEN und MITTELRÄTIEN

Verzeichniss Rätoromanischer Litteratur, 2021, Vol.20 (6, 2), p.211-213

Boehmer, Ed

2021

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GRAUBÜNDEN

Verzeichniss Rätoromanischer Litteratur, 2021, Vol.20 (6, 2), p.109-185

Boehmer, Ed

2021

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Le Patois de La Baroche

Vosgien. Rätoromanisch, 2021, Vol.7, p.61-62

Boehmer, Eduard

2021

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FRIAUL

Verzeichniss Rätoromanischer Litteratur, 2021, Vol.20 (6, 2), p.185-202

Boehmer, Ed

2021

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GRAUBÜNDEN und FRIAUL

Verzeichniss Rätoromanischer Litteratur, 2021, Vol.20 (6, 2), p.203-205

Boehmer, Ed

2021

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Differential diagnosis and treatment of girls with 46XY-karyotype and androgen insensitivity syndrome

Nederlands tijdschrift voor geneeskunde, 2001-04, Vol.145 (14), p.665

2001

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17Beta-hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations

The journal of clinical endocrinology and metabolism, 1999-12, Vol.84 (12), p.4713-4721

1999

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Pathofysiologie, diagnostiek en behandeling van chronisch hoesten

Tijdschrift voor kindergeneeskunde, 2009-10, Vol.77 (5), p.197-204

2009

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Ki-67 detects a nuclear matrix-associated proliferation-related antigen. I: Intracellular localization during interphase

Androgen insensitivity syndrome (AIS): emotional reactions of parents and adult patients to the clinical diagnosis of AIS and its confirmation by androgen receptor gene mutation analysis

Molecular Analysis of the Androgen-Receptor Gene in a Family with Receptor-Positive Partial Androgen Insensitivity: An Unusual Type of Intronic Mutation

Germ-line and somatic mosaicism in the androgen insensitivity syndrome : Implications for genetic counseling

Androgen receptor mutations

Genotype versus phenotype in families with androgen insensitivity syndrome

Molecular basis of androgen insensitivity

17β-Hydroxysteroid dehydrogenase-3 deficiency: Diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de Novo mutations

Phenotypic Variation in a Family with Partial Androgen Insensitivity Syndrome Explained by Differences in 5 Dihydrotestosterone Availability

17 -Hydroxysteroid Dehydrogenase-3 Deficiency: Diagnosis, Phenotypic Variability, Population Genetics, and Worldwide Distribution of Ancient and de Novo Mutations

ETIOLOGICAL STUDIES OF SEVERE OR FAMILIAL HYPOSPADIAS

Androgens and fetal growth

Moeilijk behandelbaar astma: diagnostiek en behandelopties

Phenotypic variation in a family with partial androgen insensitivity syndrome explained by differences in 5alpha dihydrotestosterone availability

From gene to disease; androgen receptor gene, androgen insensitivity syndrome, and spinal and bulbar muscle atrophy

Substitution of Ala564 in the first zinc cluster of the deoxyribonucleic acid (DNA)-binding domain of the androgen receptor by Asp, Asn, or Leu exerts differential effects on DNA binding

MITTELRÄTIEN

GRAUBÜNDEN und MITTELRÄTIEN

GRAUBÜNDEN

Le Patois de La Baroche

FRIAUL

GRAUBÜNDEN und FRIAUL

Differential diagnosis and treatment of girls with 46XY-karyotype and androgen insensitivity syndrome

17Beta-hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations

Pathofysiologie, diagnostiek en behandeling van chronisch hoesten

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