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Fortschritte Der Kieferorthopadie|August 1, 1991
[Cheilognathopalatoschisis: its classification and epidemiology]U HilligZeitschrift Fur Kinder- Und Jugendpsychiatrie|March 1, 1992
[A child with XYY syndrome as experienced by his mother. A report of daily journal recordings]A von Gontard, U HilligZeitschrift Fur Kinder- Und Jugendpsychiatrie|June 1, 1992
[Clinical and cytogenetic problems in diagnosis of fragile X syndrome]A von Gontard, U Hillig, D HeroldClinical Genetics|July 1, 1984
Familial pericentric inversion (14) (p11;q24) with a rec dup(q) in one offspringP Kaiser, W Förster, P Steuernagel, et al.Deutsche Medizinische Wochenschrift (1946)|February 15, 1991
[Adrenomyeloneuropathy as a cause of Addison's disease]C Baerwald, K Ehlenz, R Körber, et al.American Journal of Medical Genetics|December 10, 1999
Trisomy 2q35-q37 due to insertion of 2q material into 17q25: clinical, cytogenetic, and molecular cytogenetic characterizationB Fritz, J Müller-Navia, U Hillig, et al.European Journal of Human Genetics : EJHG|April 26, 2000
FISH mapping of the sex-reversal region on human chromosome 9p in two XY females and in primatesZ Shan, B Zabel, U Trautmann, et al.Human Genetics|April 1, 1997
Microdeletion 22q11 in complex cardiovascular malformationsY Mehraein, C F Wippermann, I Michel-Behnke, et al.Klinische Wochenschrift|June 16, 1980
[Prenatal diagnosis of alpha-1-antitrypsin phenotype. Case record and prognosis in severe alpha-antitrypsin deficiency Pi ZZ (author's transl)]S L Roth, K Havemann, G A Martini, et al.Pageof 1