G. Cobet

发表

Typing of families with classical phenylketonuria using three alleles of the Hindlll linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe

O. Riess, R. Cotton, H. Dahl, 1986 .

Cu/Zn superoxide dismutase quantification from fetal erythrocytes—an efficient confirmatory test for Down's syndrome after maternal serum screening and sonographic investigations

T. Porstmann, G. Stamminger, R. Bollmann, 1991, Prenatal diagnosis.

Typing of families with classical phenylketonuria using three alleles of the Hindiii linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe. Family typing for PKU by linked HindIII RFLP.

O. Riess, R. Cotton, H. Dahl, 1986, Clinical genetics.

Introduction of genomic diagnosis of classical phenylketonuria to the health care system of the German Democratic Republic

O. Riess, C. Coutelle, A. Speer, 1987, Clinical genetics.

Prenatal diagnosis of classical phenylketonuria by linked restriction fragment length polymorphism analysis

O. Riess, C. Coutelle, A. Speer, 1986, Prenatal diagnosis.

Linkage disequilibrium between RFLP haplotype 2 and the affected PAH allele in PKU families from the Berlin area of the German Democratic Republic

O. Riess, C. Coutelle, A. Speer, 1988, Human Genetics.

Creatine kinase isoenzyme BB in serum of healthy adults and children.

E. Egger, E. Nugel, G. Cobet, 1979, Clinica chimica acta; international journal of clinical chemistry.

[Biotinidase deficiency--a progressive metabolic disease in children with seizures and ataxia].

G. Cobet, H. Anger, K. Lorenz, 1990, Psychiatrie, Neurologie, und medizinische Psychologie.

Maternal serum alpha-fetoprotein screening for neural tube defects and other disorders using an ultramicro-ELISA

S. Tinschert, A. Horn, H. Körner, 1986, Human Genetics.

Immunochemical quantification of Cu/Zn superoxide dismutase in prenatal diagnosis of Down's syndrome

R. Grunow, R. Baehr, T. Porstmann, 1990, Human Genetics.

[Partial monosomy 21 or fetal alcohol embryopathy in a retarded boy?].

G. Laske, K. Lehmann, G. Cobet, 1993, Pädiatrie und Grenzgebiete.

ASSESSMENT OF SERUM LEVELS OF α‐1‐MICROGLOBULIN, β‐2‐MICROGLOBULIN, AND RETINOL BINDING PROTEIN IN THE FETAL BLOOD. A METHOD FOR PRENATAL EVALUATION OF RENAL FUNCTION

C. Tennstedt, R. Bollmann, B. Brux, 1996 .