B. Schulze

发表

Rare dental abnormalities seen in oculo-facio-cardio-dental (OFCD) syndrome: three new cases and review of nine patients.

D. Horn, A. Stellzig, G. Tariverdian, 1999, American journal of medical genetics.

Misclassification risk of patients with bilateral cleft lip and palate and manifestations of median facial dysplasia: A new variant of del(22q11.2) syndrome?

G. Komposch, A. Stellzig, G. Tariverdian, 2001, American journal of medical genetics.

Mosaicism in trisomy 8: phenotype differences according to tissular repartition of normal and trisomic clones.

K. Miller, M. Morlot, U. Burck, 1997, Annales de genetique.

Study of 30 patients with unexplained developmental delay and dysmorphic features or congenital abnormalities using conventional cytogenetics and multiplex FISH telomere (M-TEL) integrity assay

A. Jauch, B. Schoell, L. Kearney, 2002, Human Genetics.

Wolf-Hirschhorn syndrome: case report and review of the chromosomal aberrations associated with diaphragmatic defects.

O. Linderkamp, H. Otto, C. Sergi, 1998, Pathologica.

Chromosomal mosaicism confined to chorionic tissue

K. Miller, B. Schulze, C. Schlesinger, 1987, Prenatal diagnosis.

Tandem duplication chromosome 21 in the offspring of a ring chromosome 21 carrier.

K. Miller, B. Schulze, A. Reimer, 1987, Annales de genetique.

Paracentric inversion 14.

K. Miller, G. Raabe, B. Schulze, 1990, Annales de genetique.

Identification, by homozygosity mapping, of a novel locus for autosomal recessive congenital ichthyosis on chromosome 17p, and evidence for further genetic heterogeneity.

H. Hennies, A. Reis, P. Frossard, 2001, American journal of human genetics.