K Hinkel

Female Pseudohermaphroditism Associated with a Novel Homozygous G-to-A (V370-to-M) Substitution in the P-450 Aromatase Gene

L Wickert, U Bolkenius, Bettina Tittel et al. · Journal of Pediatric Endocrinology and Metabolism · 1998 · 71 citations

Trisomy of human chromosome 18: Molecular studies on parental origin and cell stage of nondisjunction

Thomas Eggermann, Markus M. Nöthen, B. Eiben et al. · Human Genetics · 1996 · 53 citations

Chromatin, Developmental Biology, Cytogenetics +10

Uniparental Origin of Sex Chromosome Polysomies

Isabel Lorda‐Sánchez, Franz Binkert, K Hinkel et al. · Human Heredity · 1992 · 26 citations

Fertility, Cytogenetics, Genetics +17

Selective Deficiency of Gsα and the Possible Role of Alternative Gene Products of <i>GNAS</i> in Albright Hereditary Osteodystrophy and Pseudohypoparathyroidism Type Ia

S. Thiele, Ralf Werner, Wiebke Ahrens et al. · Experimental and Clinical Endocrinology & Diabetes · 2009 · 14 citations

Prenatal diagnosis of alpha-1-antitrypsin deficiency using polymerase chain reaction (PCR). Comparison of conventional RFLP methods with PCR used in combination with allele specific oligonucleotides or RFLP analysis.

Marcia Schwartz, Kirsten Bruun Petersen, N. Gregersen et al. · PubMed · 1989 · 12 citations

Genetic Testing, Genetics, Genetic Epidemiology +16