H. U. Tietze

Genotype-phenotype correlations in Noonan syndrome

Martin Zenker, G. Buheitel, R. Rauch et al. · The Journal of Pediatrics · 2004 · 248 citations

Life Sciences, Genetics, Molecular Genetics +9

Translocation breakpoints in three patients with campomelic dysplasia and autosomal sex reversal map more than 130 kb from SOX9

Jutta Wirth, Thomas Wagner, Jobst Meyer et al. · Human Genetics · 1996 · 97 citations

Life Sciences, Genetics, Molecular Genetics +12

1,25-Dihydroxyvitamin D Resistance, Rickets, and Alopecia: Analysis of Receptors and Bioresponse in Cultured Fibroblasts from Patients and Parents*

Theresa L. Chen, Margaret Hirst, Charlotte M. Cone et al. · The Journal of Clinical Endocrinology & Metabolism · 1984 · 86 citations

Medicine, Dermatology, Endocrinology +17

Pseudohypoaldosteronism in Eight Families: Different Forms of Inheritance Are Evidence for Various Genetic Defects

Ursula Kuhnle, Meta Damkjær Nielsen, H. U. Tietze et al. · The Journal of Clinical Endocrinology & Metabolism · 1990 · 63 citations

Medicine, Endocrinology, Genetics +14

Severe skeletal dysplasia caused by undiagnosed hypothyroidism

Ulrike Hüffmeier, H. U. Tietze, Anita Rauch · European Journal of Medical Genetics · 2007 · 34 citations

Medicine, Endocrinology, Bone Metabolism +12