Year |
Citation |
Score |
2009 |
Engel W, Faust J, Wolf U. Isoenzyme polymorphism of the sorbitol dehydrogenase and the NADP‐dependent isocitrate dehydrogenases in the fish family Cyprinidae Animal Blood Groups and Biochemical Genetics. 2: 127-133. DOI: 10.1111/J.1365-2052.1971.Tb01213.X |
0.351 |
|
1995 |
Blin N, Kaiser P, Krone W, Ritter H, Rosing-Diederich I, Schroeder-Kurth TM, Vogel W, Wolf U. Assignment, structure and development of the Institute for Human Genetics (and Anthropology) of the Universities in Baden-Wurttemberg | AUFGABEN, STRUKTUR UND ENTWICKLUNG DER INSTITUTE FUR HUMANGENETIK (UND ANTHROPOLOGIE) AN DEN UNIVERSITATEN IN BADEN-WURTTEMBERG Medizinische Genetik. 7: 14-18. |
0.418 |
|
1994 |
Wagner T, Wirth J, Meyer J, Zabel B, Held M, Zimmer J, Pasantes J, Bricarelli FD, Keutel J, Hustert E, Wolf U, Tommerup N, Schempp W, Scherer G. Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9 Cell. 79: 1111-1120. PMID 8001137 DOI: 10.1016/0092-8674(94)90041-8 |
0.341 |
|
1993 |
Tommerup N, Schempp W, Meinecke P, Pedersen S, Bolund L, Brandt C, Goodpasture C, Guldberg P, Held KR, Reinwein H, Saugstad OD, Scherer G, Skjeldal O, Toder R, Westvik J, ... ... Wolf U, et al. Assignment of an autosomal sex reversal locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3-q25.1 Nature Genetics. 4: 170-174. PMID 8348155 DOI: 10.1038/ng0693-170 |
0.357 |
|
1992 |
Wolf U, Schempp W, Scherer G. Molecular biology of the human Y chromosome Reviews of Physiology Biochemistry and Pharmacology. 121: 147-213. PMID 1485072 DOI: 10.1007/Bfb0033195 |
0.366 |
|
1989 |
Scherer G, Schempp W, Baccichetti C, Lenzini E, Bricarelli FD, Carbone LDL, Wolf U. Duplication of an Xp segment that includes the ZFX locus causes sex inversion in man Human Genetics. 81: 291-294. PMID 2921042 DOI: 10.1007/BF00279008 |
0.352 |
|
1989 |
Scherer G, Schempp W, Fraccaro M, Bausch E, Bigozzi V, Maraschio P, Montali E, Simoni G, Wolf U. Analysis of two 47,XXX males reveals X-Y interchange and maternal or paternal nondisjunction Human Genetics. 81: 247-251. PMID 2921034 DOI: 10.1007/BF00278998 |
0.339 |
|
1989 |
Schempp W, Müller G, Scherer G, Bohlander SK, Rommerskirch W, Fraccaro M, Wolf U. Localization of Y chromosome sequences and X chromosomal replication studies in XX males Human Genetics. 81: 144-148. PMID 2912884 DOI: 10.1007/BF00293890 |
0.361 |
|
1986 |
Maserati E, Waibel F, Weber B, Fraccaro M, Gal A, Pasquali F, Schempp W, Scherer G, Vaccaro R, Weissenbach J, Wolf U. A 45,X male with a Yp/18 translocation Human Genetics. 74: 126-132. PMID 2876945 DOI: 10.1007/BF00282075 |
0.38 |
|
1985 |
Schempp W, Weber B, Serra A, Neri G, Gal A, Wolf U. A 45,X male with evidence of a translocation of Y euchromatin onto chromosome 15 Human Genetics. 71: 150-154. PMID 4043963 DOI: 10.1007/BF00283372 |
0.385 |
|
1983 |
Wolf U. X-linked genes and gonadal differentiation Differentiation. 23: S104-106. PMID 6444165 DOI: 10.1007/978-3-642-69150-8_18 |
0.345 |
|
1982 |
Fraccaro M, Mayerová A, Wolf U, Bühler E, Gebauer J, Gilgenkrantz S, Lindsten J, Lo Curto F, Ritzen EM. Correlation between the number of sex chromosomes and the H-Y antigen titer Human Genetics. 61: 135-140. PMID 7129440 DOI: 10.1007/BF00274203 |
0.402 |
|
1982 |
Wiberg U, Mayerová A, Müller U, Fredga K, Wolf U. X-linked genes of the H-Y antigen system in the wood lemming (Myopus schisticolor) Human Genetics. 60: 163-166. PMID 7042534 DOI: 10.1007/BF00569705 |
0.316 |
|
1981 |
Passarge E, Wolf U. Genetic heterogeneity of XY gonadal dysgenesis (Swyer syndrome): H-Y antigen-negative XY gonadal dysgenesis associated with inflammatory bowel syndrome American Journal of Medical Genetics. 8: 437-441. PMID 7246614 DOI: 10.1002/Ajmg.1320080409 |
0.369 |
|
1981 |
Bricarelli FD, Fraccaro M, Lindsten J, Müller U, Baggio P, Carbone LDL, Hjerpe A, Lindgren F, Mayerová A, Ringertz H, Ritzén EM, Rovetta DC, Sicchero C, Wolf U. Sex-reversed XY females with campomelic dysplasia are H-Y negative Human Genetics. 57: 15-22. PMID 7196380 DOI: 10.1007/BF00271160 |
0.307 |
|
1981 |
Wolf U. Genetic aspects of H-Y antigen Human Genetics. 58: 25-28. PMID 7026414 DOI: 10.1007/BF00284144 |
0.401 |
|
1980 |
Wolf U, Fraccaro M, Mayerová A, Hecht T, Zuffardi O, Hameister H. Turner syndrome patients are H-Y positive Human Genetics. 54: 315-318. PMID 7399526 DOI: 10.1007/BF00291575 |
0.332 |
|
1980 |
Wolf U, Fraccaro M, Mayerová A, Hecht T, Maraschio P, Hameister H. A gene controlling H-Y antigen on the X chromosome - Tentative assignment by deletion mapping to Xp223 Human Genetics. 54: 149-154. PMID 7390489 DOI: 10.1007/BF00278963 |
0.352 |
|
1977 |
Krone W, Wolf U. Chromosome variation and gene action Hereditas. 86: 31-35. PMID 903250 DOI: 10.1111/J.1601-5223.1977.Tb01209.X |
0.396 |
|
1973 |
Engel W, Schmidtke J, Vogel W, Wolf U. Genetic polymorphism of lactate dehydrogenase isoenzymes in the carp (Cyprinus carpio) apparently due to a "null allele" Biochemical Genetics. 8: 281-289. PMID 4701994 DOI: 10.1007/BF00486181 |
0.307 |
|
1971 |
Zenzes MT, Wolf U. Pairing behaviour of the sex chromosomes during male meiosis of Microtus agrestis | Paarungsverhalten der Geschlechtschromosomen in der männlichen Meiose von Microtus agrestis Chromosoma. 33: 41-47. PMID 5574764 DOI: 10.1007/BF00326382 |
0.355 |
|
1971 |
Chaudhuri JP, Vogel W, Voiculescu I, Wolf U. A simplified method of demonstrating Giemsa-Band pattern in human chromosomes Human Genetics. 14: 83-84. PMID 5144910 DOI: 10.1007/BF00273042 |
0.315 |
|
1971 |
Hoehn H, Wolf U, Schumacher H, Wehinger H. A Chromosome 13q+in a patient with characteristics of the trisomy 13 syndrome Humangenetik. 13: 34-42. PMID 5115887 DOI: 10.1007/BF00446411 |
0.399 |
|
1970 |
Engel W, Bender K, Kadir S, Op't Hof J, Wolf U. [The genetics of 6-PGD (EC; 1.1.1.44) in various mammals. I. Studies on 6 species of Microtinae, Rodentia, Isoenzyme polymorphism and family studies in Microtus oeconomus and Microtus ochrogaster]. Humangenetik. 10: 151-7. PMID 5507049 DOI: 10.1007/Bf00295514 |
0.51 |
|
1970 |
Krone W, Wolf U, Goedde HW, Baitsch H. Elevated galactokinase activity in blood cells of patients with G-trisomy: a belated correction. Humangenetik. 11: 81-2. PMID 5490360 DOI: 10.1007/BF00296310 |
0.595 |
|
1970 |
Engel W, Hof JOt, Wolf U. Sorbitol dehydrogenase isozymes in clupeoid fish: a further example of gene duplication through polyploid evolution | Genduplikation durch polyploide Evolution: die Isoenzyme der Sorbitdehydrogenase bei herings- und lachsartigen Fischen (Isospondyli) Human Genetics. 9: 157-163. PMID 5423928 DOI: 10.1007/BF00278931 |
0.306 |
|
1970 |
Wolf U, Engel W, Faust J. The mechanism of diploidization in vertebrate evolution: Coexistence of tetrasomic and disonic gene loci for the isocitrate dehydrogenases in trout (Salmo irideus) | Zum Mechanismus der Diploidisierung in der Wirbeltierevolution: Koexistenz von tetrasomen und disomen Genloci der Isocitrat-Dehydrogenasen bei der Regenbogenforelle (Salmo irideus) Human Genetics. 9: 150-156. PMID 4393176 DOI: 10.1007/BF00278930 |
0.3 |
|
1969 |
Wolf U, Hepp D. [DNA replication pattern of somatic chromosomes of Cricetus cricetus (L)]. Chromosoma. 18: 438-48. PMID 6012391 DOI: 10.1007/BF00332547 |
0.367 |
|
1969 |
Klose J, Wolf U, Hitzeroth H, Ritter H, Ohno S. Polyploidization in the fish family Cyprinidae, order Cypriniformes - II. Duplication of the gene loci coding for lactate dehydrogenase (E.C.: 1.1.1.27) and 6-phosphogluconate dehydrogenase (E.C.: 1.1.1.44) in various species of Cyprinidae Human Genetics. 7: 245-250. PMID 5800706 DOI: 10.1007/BF00273174 |
0.484 |
|
1969 |
Wolf U, Ritter H, Atkin NB, Ohno S. Polyploidization in the fish family Cyprinidae, order Cypriniformes - I. DNA-Content and chromosome sets in various species of Cyprinidae Human Genetics. 7: 240-244. PMID 5800705 DOI: 10.1007/BF00273173 |
0.361 |
|
1969 |
Ritter H, Baitsch H, Wolf U. [On the formal genetics of isoenzymes, using 6-PGD (EC:1.1.1.44) as an example]. Humangenetik. 7: 1-4. PMID 5770376 DOI: 10.1007/BF00278686 |
0.661 |
|
1969 |
Op't Hof J, Wolf U, Krone W. Studies on isozymes of sorbitol dehydrogenase in some vertebrate species Human Genetics. 8: 178-182. PMID 5391959 DOI: 10.1007/BF00280570 |
0.308 |
|
1969 |
Wolf U, Engel W, Baitsch H. [Genetics of the YY syndrome]. BeiträGe Zur Gerichtlichen Medizin. 26: 251-5. PMID 5366503 |
0.59 |
|
1969 |
Bender K, Reinwein H, Gorman LZ, Wolf U. [Familial 2-C translocation: 46,XYt(2p-;Cp+) and 46,XXCp+]. Humangenetik. 8: 94-104. PMID 5365588 DOI: 10.1007/Bf00295832 |
0.474 |
|
1969 |
Ritter H, Engel W, Op't Hof J, Wolf U. Studies of protein polymorphism in a family exhibiting a variety of chromosome aberrations | Untersuchungen von Proteinpolymorphismen an einer Familie mit gehäuften Chromosomenaberrationen Human Genetics. 8: 33-38. PMID 5364421 DOI: 10.1007/BF00286753 |
0.355 |
|
1968 |
Engel W, Merker H, Schneider G, Wolf U. Clonal occurrence of a chromosome Dq-in myelosclerosis with myeloid metaplasia Human Genetics. 6: 335-337. PMID 5713619 DOI: 10.1007/BF00286802 |
0.355 |
|
1968 |
Engel W, Reinwein H, Bombel D, Ritter H, Wolf U. Multiple malformations in a girl of karyotype 46, XY, 17q+ | Multiple Mißbildungen bei einem Mädchen mit dem Karyotypus 46, XY, 17q+ Human Genetics. 6: 311-325. PMID 5713617 DOI: 10.1007/BF00286800 |
0.563 |
|
1968 |
Engel W, Op't Hof J, Ritter H, Wolf U. Mapping of human chromosomes - II. Exclusion of gene loci in deficiency 5p | Zur Frage der Zuordnung von Loci - II. Lokalisierungsausschlüsse bei Defizienzen 5p Human Genetics. 6: 279-280. PMID 5709088 DOI: 10.1007/Bf00291874 |
0.522 |
|
1968 |
Böckelmann W, Wolf U, Ritter H. Polymorphism of the phosphotransferases adenylate kinase and pyruvate kinase - Existence of a common subunit? Human Genetics. 6: 78-83. PMID 5699898 DOI: 10.1007/BF00287158 |
0.455 |
|
1968 |
Wille B, Bender K, Wolf U, Ritter H. [On the population genetics of acid phosphatase in erythrocytes (E C 3.1.3.2.): phenotype and allele frequency in Southwestern Germany]. Humangenetik. 5: 274-7. PMID 5662660 DOI: 10.1007/Bf00281966 |
0.593 |
|
1968 |
Klose J, Wolf U, Hitzeroth H, Ritter H, Atkin NB, Ohno S. Duplication of the LDH gene loci by polyploidization in the fish order Clupeiformes Human Genetics. 5: 190-196. PMID 5662651 DOI: 10.1007/BF00281954 |
0.527 |
|
1968 |
Wolf U, Reinwein H, Lohmann H. Zur Genetik und Klinik kleiner Chromosomenaberrationen - Ein Chromosom Gp+h und ein Chromosom Gs+ in einer Familie Human Genetics. 5: 107-118. PMID 5662646 DOI: 10.1007/BF00278671 |
0.401 |
|
1968 |
Reinwein H, Ritter H, Wolf U. Deletion of short arm of a chromosome 18 (46, XX, 18 p-). Humangenetik. 5: 72-3. PMID 5585063 DOI: 10.1007/BF00286215 |
0.549 |
|
1968 |
Wolf U, Reinwein H, Gorman LZ, Künzer W. Deletion on long arm of a chromosome 18 (46, XX, 18 q-). Humangenetik. 5: 70-1. PMID 5585062 DOI: 10.1007/BF00286214 |
0.311 |
|
1968 |
Pera F, Wolf U. [DNA-replication and morphology of X-chromosomes during the synthesis period in Microtus agretis]. Chromosoma. 22: 378-89. PMID 4169561 DOI: 10.1007/BF00319881 |
0.348 |
|
1967 |
Bender K, Ritter H, Wolf U. [On the problem of assigning genes to definite human autosomes with the aid of chromosome aberrations]. Humangenetik. 4: 85-103. PMID 4865216 DOI: 10.1007/Bf00291253 |
0.65 |
|
1967 |
Engel W, Krone W, Wolf U. Die wirkung von thioguanin, hydroxylamin unde 5-bromdesoxyuridin auf menschliche chromosomen in vitro Mutation Research. 4: 353-368. PMID 4228103 DOI: 10.1016/0027-5107(67)90030-9 |
0.365 |
|
1967 |
Reinwein H, Gorman LZ, Wolf U. Defizienz am langen Arm eines Chromosoms Nr. 18 (46, XX, 18 q-) Zeitschrift F�R Kinderheilkunde. 101: 152-164. DOI: 10.1007/BF00439697 |
0.372 |
|
1967 |
Castro-Sierra E, Gorman LZ, Merker H, Obrecht P, Wolf U. Clinical and cytogenetic findings in the terminal phase of chronic myelogenous leukaemia Human Genetics. 4: 62-73. DOI: 10.1007/BF00279181 |
0.302 |
|
1966 |
Reinwein H, Schilli W, Ritter H, Brehme H, Wolf U. [Studies on a family with orofaciodigital syndrome]. Humangenetik. 2: 165-77. PMID 5916636 DOI: 10.1007/BF00291516 |
0.481 |
|
1966 |
Wolf U, Reinwein H. Chromosomenmosaik C-Trisomie/normal Human Genetics. 1: 686-687. DOI: 10.1007/BF00281057 |
0.337 |
|
1965 |
WOLF U, PORSCH R, BAITSCH H, REINWEIN H. DELETION ON SHORT ARMS OF A B-CHROMOSOME WITHOUT "CRI DU CHAT" SYNDROME. Lancet (London, England). 1: 769. PMID 14255266 |
0.63 |
|
1965 |
Wolf U, Reinwein H, Porsch R, Schröter R, Baitsch H. [Deficiency on the short arms of a chromosome No. 4]. Humangenetik. 1: 397-413. PMID 5868696 DOI: 10.1007/BF00279119 |
0.656 |
|
1965 |
Bettecken F, Reinwein H, Künzer W, Wolf U, Baitsch H. [Clinical and genetic studies of a patient with crying cat syndrome]. Deutsche Medizinische Wochenschrift (1946). 90: 2008-13. PMID 5833954 DOI: 10.1055/s-0028-1113464 |
0.587 |
|
1965 |
Krone W, Wolf U, Goedde HW, Baitsch H. [Studies on the activity of galactokinase in the blood of normal persons and of patients with GDo trisomy]. Humangenetik. 1: 279-88. PMID 4223835 DOI: 10.1007/BF00395658 |
0.594 |
|
1964 |
WOLF U, BAITSCH H, KUENZER W, REINWEIN H. [FAMILIAL OCCURRENCE OF AN ABNORMAL D-CHROMOSOME]. Cytogenetics. 3: 112-23. PMID 14190610 |
0.618 |
|
1964 |
KRONE W, WOLF U, GOEDDE HW, BAITSCH H. ENHANCEMENT OF ERYTHROCYTE-GALACTOKINASE ACTIVITY IN LANGDON-DOWN TRISOMY. Lancet (London, England). 2: 590. PMID 14172380 |
0.561 |
|
1964 |
Baitsch H, Wolf U. [The utilization of chromosomal changes for the diagnosis of radiation injury in man]. Strahlenschutz in Forschung Und Praxis. 4: 259-74. PMID 5878291 |
0.589 |
|
1963 |
Wolf U, Brehme H, Baitsch H, Künzer W, Reinwein H. APLASIA OF THE DERMAL RIDGE PATTERNS IN MONGOLISM (G-TRISOMY) The Lancet. 282: 887. |
0.547 |
|
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