Search

Your search keyword '"Tünte, W."' showing total 30 results
Start Over Author "Tünte, W."
30 results on '"Tünte, W."'

8. Linkage analysis in X-linked adrenoleukodystrophy and application in post-and prenatal diagnosis.

Author

Oost, B., Zandvoort, P., Tünte, W., Brunner, H., Hoogeboom, A., Maaswinkel-Mooy, P., Bakkeren, J., Hamel, B., and Ropers, H.

Abstract

We have performed linkage analysis with the DNA markers DXS52 and the clotting factor VIII gene (F8C), in several large families with X-linked adrenoleukodystrophy (ALD). The tight linkage to DXS52 could be extended giving a maximal LOD score of 22.5 at 1 cM. F8C was also tightly linked to ALD with a maximal LOD score of 7.8 without recombination. Multipoint linkage analysis with the markers DXS304, DXS52, and F8C indicated that both the gene for ALD and for F8C are distal to DXS52. In four patients with ALD, no major structural rearrangement in the Xqter region was observed; in particular, there were no abnormalities in the vision blindness genes. DNA analysis appeared to be of use in determination of the carrier status of females at risk, for the determination of the origin of the mutation in a particular family, and for prenatal diagnosis. [ABSTRACT FROM AUTHOR]

Published
1991
Full Text
View/download PDF

15. [Placental chorioangioma and fetal abnormalities].

Author

Glaser D, Jünemann A, Tünte W, Flotmann U, Hanewinkel H, and Robke K

Subjects
Abortion, Induced, Adult, Female, Humans, Placenta pathology, Placental Insufficiency pathology, Pregnancy, Abnormalities, Multiple pathology, Hemangioma pathology, Placenta Diseases pathology
Abstract

We report on a postpartally decreased girl with several malformations: turricephalus, deep root of the nose, prognathism, choanal atresia, low-set dysplastic ears, fourth additional blood vessel originating from the thoracic aorta. Nearly 70% of the placenta consisted of multiple chorioangiomas. A possible correlation between fetal malformations and placental chorangiomas is discussed. There is no valuable reference to a hereditary component in the development of chorioangiomas.

Published
1988
Full Text
View/download PDF

16. [Acrocephalopolysyndactyly (type II (McKusick) acrocephalosyndactyly or Carpenter's syndrome. Report on 4 cases and an observation of the syndrome of Marshall-Smith (author's transl)].

Author

Pfeiffer RA, Seemann KB, Tünte W, Gussone J, and Klemm E

Subjects
Abnormalities, Multiple diagnosis, Acrocephalosyndactylia diagnostic imaging, Acrocephalosyndactylia genetics, Adolescent, Child, Female, Heart Defects, Congenital complications, Humans, Infant, Infant, Newborn, Male, Radiography, Acrocephalosyndactylia diagnosis
Abstract

Four observations of Carpenter's Syndrome, two siblings and two unrelated children, and a case of Marshall-Smith's Syndrome are reported, all sharing duplication of the terminal phalanx of the big toe and a dyskephaly. Carpenter's Syndrome has been noted in at least 27 cases inheritance; is autosomalcessive. Main features are: oxycephaly, odd facies, brachyclinosyndactyly of the hands, polysyndactyly of the feet, cardiac malformation. The question is to be answered whether all cases are genetically identical.

Published
1977

17. [Incidence of congenital biliary atresia].

Author

Tünte W

Subjects
Biliary Tract Diseases etiology, Biliary Tract Diseases pathology, Birth Order, Humans, Infant, Rural Population, Seasons, Sex Factors, Bile Ducts abnormalities, Biliary Tract Diseases congenital
Published
1968

20. Supernumerary chromosomes (trisomies) and maternal age.

Author

Lenz W, Pfeiffer RA, and Tünte W

Subjects
Adolescent, Adult, Chromosome Disorders, Female, Humans, Infant, Newborn, Middle Aged, Pregnancy, Chromosome Aberrations epidemiology, Maternal Age, Trisomy epidemiology
Published
1967

22. [Mirror immage duplication of ulna and ulnar hand part in absent radius ("mirror hand")].

Author

Tünte W and Kersting D

Subjects
Arm diagnostic imaging, Child, Child, Preschool, Congenital Abnormalities genetics, Female, Humans, Infant, Infant, Newborn, Male, Pattern Recognition, Automated, Radiography, Skin Abnormalities, Congenital Abnormalities etiology, Hand Deformities, Acquired, Radius abnormalities, Ulna abnormalities
Published
1967

24. [Anal atresia in twins].

Author

Tünte W

Subjects
Anus, Imperforate complications, Female, Humans, Infant, Newborn, Male, Ribs abnormalities, Spine abnormalities, Thumb abnormalities, Abnormalities, Multiple, Anus, Imperforate genetics, Diseases in Twins
Published
1969

25. [The popliteal pterygium syndrome. A dominant autosomal malformation syndrome].

Author

Pfeiffer RA, Tünte W, and Reinken M

Subjects
Adult, Child, Child, Preschool, Female, Genes, Dominant, Humans, Infant, Male, Abnormalities, Multiple genetics, Chromosome Aberrations, Chromosome Disorders, Cleft Lip complications, Cleft Palate complications, Genitalia abnormalities, Knee abnormalities, Skin Abnormalities, Syndactyly complications
Published
1970

29. [The oro-facial-digital syndrome. Symptoms and prognosis].

Author

Majewski F, Lenz W, Pfeiffer RA, Tünte W, and Müller H

Subjects
Alopecia complications, Brain abnormalities, Child, Child, Preschool, Cleft Palate complications, Facial Expression, Female, Fingers abnormalities, Humans, Hydrocephalus complications, Infant, Infant, Newborn, Middle Aged, Orofaciodigital Syndromes diagnosis, Pedigree, Polycystic Kidney Diseases complications, Syndactyly complications, Tongue abnormalities, Tongue Neoplasms complications, Tooth Abnormalities complications, Abnormalities, Multiple genetics, Intellectual Disability genetics
Published
1972

Catalog

Books, media, physical & digital resources
See catalog results