M. Zankl

发表

Mosaic tetraploidy in a liveborn infant with features of the DiGeorge anomaly

B. Wullich, W. Henn, A. Ermis, 1991, Clinical genetics.

Dermatoglyphic peculiarities in Down's syndrome detection of mosaicism and balanced translocation carriers.

K. Zang, H. Zankl, M. Zankl, 1981, Human genetics. Supplement.

Dermatoglyphic studies in parents of children with trisomy 21: detection of hidden mosaicism and its role in genetic counselling.

K. Zang, H. Zankl, M. Zankl, 1982, Progress in clinical and biological research.

Distal 2q duplication: report of two familial cases and an attempt to define a syndrome.

K. Zang, G. Dockter, H. Zankl, 1979, American journal of medical genetics.

Cocultivation studies with cells of patients bearing fragile X chromosomes

H. Zankl, M. Zankl, Gertrud Eberle, 2004, Human Genetics.

Partial trisomie 5q: Three different phenotypes depending on different duplication segments

K. Zang, M. Zankl, A. Rodewald, 2004, Human Genetics.

Dermatoglyphic peculiarities in families with X‐linked mental retardation and fragile site Xq27: a collaborative study

U. Langenbeck, U. Froster-Iskenius, R. Wegner, 1986, Clinical genetics.

New chromosomal dysmorphic syndromes

J. Murken, M. Zankl, A. Rodewald, 1981, European Journal of Pediatrics.

The dermatoglyphic pattern of the trisomy 9p syndrome

M. Zankl, A. Rodewald, S. Stengel‐Rutkowskii, 1979, Clinical genetics.

Progressive hydrocephalus in two members of a family with autosomal dominant Noonan phenotype

K. Zang, W. Henn, A. Lindinger, 1997, Clinical dysmorphology.

Dermatoglyphs in carriers of a balanced 15;21 translocation.

K. Zang, H. Zankl, M. Zankl, 1980, Journal of medical genetics.

Inheritance of microtia and aural atresia in a family with five affected members

K. Zang, M. Zankl, 1979, Clinical genetics.

Interstitial de novo deletion of the long arm of chromosome 5: Mapping of 5q bands associated with particular malformations

K. Zang, F. Sitzmann, M. Zankl, 1982, Clinical genetics.

Spastic disorder in patients with hereditary multiple exostoses, but without spinal cord compression: a new syndrome?

R. Kloss, G. Hamann, K. Schimrigk, 1992, Journal of medical genetics.

Molecular analysis of the L1CAM gene in patients with X-linked hydrocephalus demonstrates eight novel mutations and suggests non-allelic heterogeneity of the trait.

J. Schröder, A. Gal, U. Orth, 1997, American journal of medical genetics.

The expression of fragile X chromosomes in members of the same family at different times of examination

H. Zankl, M. Zankl, Gertrud Eberle, 1982, Human Genetics.

SOURCES OF ERROR IN FRAGILE-X DETERMINATION

H. Zankl, M. Zankl, D. Soudek, 1981, The Lancet.

[Arterial tortuosity syndrome].

A. Lindinger, H. Limbach, M. Faiyaz-ul-Haque, 2020, Klinische Padiatrie.