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89
Referenced
154
-
Althoff, H.: Zur Panmyelopathie Fanconi als Zustandsbild multipler Abartung. Z. Kinderheilk. 72, 267?292 (1953)
(
10.1007/BF00438604
) / Z. Kinderheilk. by H. Althoff (1953) -
Arlt, H. G.: Über den Einfluß hormoneller Faktoren auf den Verlauf der konstitutionellen Panmyelopathie mit multiplen Abartungen (Fanconi-Syndrom). Z. Kinderheilk. 77, 336?348 (1955)
(
10.1007/BF00438784
) / Z. Kinderheilk. by H. G. Arlt (1955) - Atai, P.: Cytogenetische Untersuchung bei einem Fall von Fanconi-Anämie. Med. Diss., Düsseldorf 1972
- Bätke, W.: Mißbildungen bei der Fanconi-Panmyelopathie. Med. Diss., Hamburg 1964
- Baumann, Th.: Konstitutionelle Panmyelophthise mit multiplen Abartungen (Fanconi-Syndrom). Ann. Paediat. 177, 65?76, 142?174 (1951) / Ann. Paediat. by Th. Baumann (1951)
- Beard, M. E. J., Young, D. E., Bateman, G. T., McCarthy, G. T., Smith, M. E., Sinclair, L., Franklin, A. W., Bodley Scott, R.: Fanconi's anaemia. Quart. J. Med. 42, 403?422 (1973) / Quart. J. Med. by M. E. J. Beard (1973)
-
Beautyman, W.: A case of Fanconi's anaemia. Arch. Dis. Childh. 26, 238?240 (1951)
(
10.1136/adc.26.127.238
) / Arch. Dis. Childh. by W. Beautyman (1951) - Bernard, J., Mathé, G., Najean, Y.: Contribution à l'étude clinique et physiopathologique de la maladie de Fanconi. Rev. franç. Étud. clin. biol. 3, 599?612 (1958) / Rev. franç. Étud. clin. biol. by J. Bernard (1958)
-
Bloom, G. E., Warner, S., Gerald, P. S., Diamond, L. K.: Chromosome abnormalities in constitutional aplastic anemia. New Engl. J. Med. 274, 8?14 (1966)
(
10.1056/NEJM196601062740102
) / New Engl. J. Med. by G. E. Bloom (1966) - Boivin, P., Bousser, J., Robineaux, R., Pringuet, C.: Pancytopénie avec malformations multiples (Syndrome de Fanconi). Arch. franç. Pédiat. 15, 1289?1321 (1958) / Arch. franç. Pédiat. by P. Boivin (1958)
-
Buchem, F. S. P. van, Samson, N., Nieweg, H. O.: Familial pancytopenia with congential abnormalities (Fanconi syndrome). Acta med. scand. 149, 19?29 (1954)
(
10.1111/j.0954-6820.1954.tb11408.x
) / Acta med. scand. by F. S. P. Buchem van (1954) - Cassimos, C., Zannos, L.: Congenital hypoplastic anemia associated with multiple development defects (Fanconi's syndrome). Amer. J. Dis. Child. 84, 347?350 (1952) / Amer. J. Dis. Child. by C. Cassimos (1952)
-
Chung, C. S., Robinson, O. W., Morton, N. E.: A note on deafmutism. Ann. hum. Genet. 23, 357?366 (1958/59)
(
10.1111/j.1469-1809.1959.tb01479.x
) / Ann. hum. Genet. by C. S. Chung (1958/59) -
Cowdell, R. H., Phizackerley, P. J. R., Pyke, D. A.: Constitutional anemia (Fanconi's syndrome) and leukemia in two brothers. Blood 10, 788?801 (1955)
(
10.1182/blood.V10.8.788.788
) / Blood by R. H. Cowdell (1955) - Crisalli, M., Sansone, G.: Constitutional infantile panmyelopathy with multiple malformations (?Fanconi anemia?). First Italian report. Helv. paediat. Acta 7, 299?308 (1952) / Helv. paediat. Acta by M. Crisalli (1952)
-
Dacie, J. V., Gilpin, A.: Refractory anaemia (Fanconi type). Its incidence in three members of one family with in one case a relationship to chronic haemolytic anaemia nocturnal haemoglobinuria (Marchiafava-Micheli disease or ?nocturnal haemoglobinuria?). Arch. Dis. Childh. 19, 155?161 (1944)
(
10.1136/adc.19.100.155
) / Arch. Dis. Childh. by J. V. Dacie (1944) -
Dawson, J. P.: Congenital pancytopenia associated with multiple congenital anomalies (Fanconi type). Pediatrics 15, 325?333 (1955)
(
10.1542/peds.15.3.325
) / Pediatrics by J. P. Dawson (1955) - Debray, J., Najean, Y.: Etude clinique et hématologique d'un cas de maladie de Fanconi. Path. Biol. 7, 1875?1880 (1959) / Path. Biol. by J. Debray (1959)
- Delâge, J. M.: Pancytopénia familiale. Laval méd. 21, 334?350 (1956) / Laval méd. by J. M. Delâge (1956)
- Demirag, B.: A propos d'un cas d'anémie hypoplastique avec malformations congénitales miltiples (Anémie de Fanconi). Helv. paediat. Acta 7, 296?298 (1952) / Helv. paediat. Acta by B. Demirag (1952)
- Emile-Weil, P.: Myelose aplasique infantile familiale avec malformations et troubles endocriniens. Contribution à l'étude du syndrome de Fanconi. Sang 12, 369?389 (1938) / Contribution à l'étude du syndrome de Fanconi. Sang by P. Emile-Weil (1938)
-
Fairburn, E. A., Burgen, A. S. V.: The skin lesions of monocytic leukaemia. Brit. J. Cancer 1, 352?362 (1938)
(
10.1038/bjc.1947.32
) / Brit. J. Cancer by E. A. Fairburn (1938) - Fanconi, G.: Familiäre infantile perniziosaartige Anämie (perniziöses Blutbild und Konstitution). Jb. Kinderheilk. 117, 257?280 (1927) / Jb. Kinderheilk. by G. Fanconi (1927)
- Fanconi, G.: Die familiäre Panmyelopathie. Schweiz. med. Wschr. 94, 1309?1318 (1964) / Schweiz. med. Wschr. by G. Fanconi (1964)
- Fanconi, G.: Familial constitutional panmyelopathy, Fanconi's anemia (F.A.). I. Clinical aspects. Semin. Hemat. 4, 233?240 (1967) / Semin. Hemat. by G. Fanconi (1967)
- Feller, W.: An introduction to probability theory and its applications. New York: Wiley 1950 / An introduction to probability theory and its applications by W. Feller (1950)
-
Finney, D. J.: The truncated binomial distribution. Ann. Eugen. (Lond.) 14, 319?328 (1947/49)
(
10.1111/j.1469-1809.1947.tb02410.x
) / Ann. Eugen. (Lond.) by D. J. Finney (1947/49) -
Garriga, S., Crosby, W. H.: The incidence of leukemia in families of patients with hypoplasia of the marrow. Blood 14, 1008?1014 (1959)
(
10.1182/blood.V14.9.1008.1008
) / Blood by S. Garriga (1959) - Gasser, C.: Panmyelopathien im Kindesalter. Beitrag zur Fanconi-Anämie. Helv. paediat. Acta 16, 752?794 (1961) / Beitrag zur Fanconi-Anämie. Helv. paediat. Acta by C. Gasser (1961)
- Genz, H.: Klinische Beobachtungen und Untersuchungen bei einem Fall von Fanconi-Anämie. Arch. Kinderheilk. 145, 237?242 (1942) / Arch. Kinderheilk. by H. Genz (1942)
- Germain, D., Requin, Ch., Robert, J., Viala, J. J., Freycon, F.: Les anomalies chromosomique dans l'anémie de Fanconi. A propos de 6 observations personelles. Pédiatrie 23, 153?167 (1968) / Pédiatrie by D. Germain (1968)
- German, J.: Genes which increase chromosomal instability in somatic cells and predispose to cancer, Ch. 2. In: Progr. med. Genet. 8, 61?101 (1972)
-
German, J.: Oncogenetic implications of chromosomal instability. Hosp. Pract. 8, 93?104 (1973)
(
10.1080/21548331.1973.11706348
) / Hosp. Pract. by J. German (1973) -
Gmyrek, D., Syllm-Rapoport, I.: Zur Fanconi-Anämie (FA). Analyse von 129 beschriebenen Fällen. Z. Kinderheilk. 91, 297?337 (1964)
(
10.1007/BF00439778
) / Z. Kinderheilk. by D. Gmyrek (1964) -
Gmyrek, D., Witkowski, R., Syllm-Rapoport, I., Jacobasch, G.: Chromosomenaberrationen und Stoffwechselstörungen der Blutzellen bei Fanconi-Anämie vor und nach Übergang in Leukose am Beispiel einer Patientin. Dtsch. med. Wschr. 92, 1701?1707 (1967)
(
10.1055/s-0028-1106028
) / Dtsch. med. Wschr. by D. Gmyrek (1967) - Grislain, J.-R., Lemoine, P., Martouzet: Nanisme type Fanconi avec myélose aplasique terminale. Arch. franç. Pédiat. 14, 415?422 (1957) / Arch. franç. Pédiat. by J.-R. Grislain (1957)
- Grouchy de, J., de Nava, C., Marchand, J. C., Feingold, J., Turleau, C.: Etudes cytogénétique et biochimique de huit cas d'anémie de Fanconi. Ann. Génét. 15, 29?40 (1972) / Ann. Génét. by J. Grouchy de (1972)
-
Gunz, F. W.: Unpublished communication (1973)
(
10.1016/S0031-3025(16)39227-3
) -
Haldane, J. B. S., Smith, C. A. B.: A simple exact test for birth order effect. Ann. Eugen. (Lond.) 14, 117?124 (1947?1949)
(
10.1111/j.1469-1809.1947.tb02383.x
) / Ann. Eugen. (Lond.) by J. B. S. Haldane (1947?1949) -
Higashi, O., Koseki, E., Higuchi, M.: A case of Fanconi's syndrome with a study of peroxydase activity of the erythron. Arch. Dis. Childh. 28, 359?362 (1953)
(
10.1136/adc.28.141.359
) / Arch. Dis. Childh. by O. Higashi (1953) -
Hirschman, R. J., Shulman, N. R., Abuelo, J. G., Whang-Peng, J.: Chromosomal aberrations in two cases of inherited aplastic anemia with unusual clinical features. Ann. intern. Med. 71, 107?117 (1969)
(
10.7326/0003-4819-71-1-107
) / Ann. intern. Med. by R. J. Hirschman (1969) - Hjorth, P.: T tilfaelde af konstitutionel, infantil anaemi. Nord. med. (Hospitalstid) 7, 1313?1317 (1940) / Nord. med. (Hospitalstid) by P. Hjorth (1940)
- Hoefnagel, D., Sullivan, M., Mc Intyre, O. R., Gray, J. A., Storrs, R. C.: Panmyelopathy with congential anomalies (Fanconi) in two cousins. Helv. paediat. Acta 21, 230?238 (1966) / Helv. paediat. Acta by D. Hoefnagel (1966)
- Imerslund, O.: Hypoplastik anemi med multiple misdannelser (Fanconi-anemi). Nord. Med. 50, 1301?1314 (1953) / Nord. Med. by O. Imerslund (1953)
- Kaelin, A.: Statistische Prüf- und Schätzverfahren für die relative Häufigkeit von Merkmalsträgern in Geschwisterreihen bei einem der Auslese unterworfenen Material mit Anwendung auf das Retinagliom. Arch. Klaus-Stift. Vererb.-Forsch. 30, 263?485 (1955) / Arch. Klaus-Stift. Vererb.-Forsch. by A. Kaelin (1955)
- Kessel, I., Cohen, H.: A case of Fanconi's anemia. S. Afr. med. J. 27, 883?884 (1953) / S. Afr. med. J. by I. Kessel (1953)
-
Kunz, H. W.: Hypoplastic anemia with multiple congenital defects (Fanconi syndrome). Pediatrics 10, 286?292 (1952)
(
10.1542/peds.10.3.286
) / Pediatrics by H. W. Kunz (1952) -
Levy, W.: Aplastic anemia in siblings with multiple congenital anomalies (the Fanconi type). J. Paediat. 40, 24?41 (1952)
(
10.1016/S0022-3476(52)80231-8
) / J. Paediat. by W. Levy (1952) -
Lieber, E., Hsu, L., Spitler, L., Fudenberg, H. H.: Cytogenetic findings in a parent of a patient with Fanconi's anemia. Clin. Genet. 3, 357?363 (1972)
(
10.1111/j.1399-0004.1972.tb01468.x
) / Clin. Genet. by E. Lieber (1972) -
Loughman, W. D.: Cytogenetics and Fanconi's anemia. Experimental and other studies of a family. Diss., Berkeley (USA) 1973
(
10.2172/4472412
) - Lynch, M. J., Sherman, L., Elliott, F. G.: Fanconi's anemia (aplastic anaemia with congenital abnormalities). Canad. med. Ass. J. 71, 273?276 (1954) / Canad. med. Ass. J. by M. J. Lynch (1954)
- McAlpine, S. G.: Familial hypoplastic anaemia with congenital abnormalities (Fanconi's syndrome): report of a case. Glasg. med. J. 35, 46?50 (1954) / Glasg. med. J. by S. G. McAlpine (1954)
-
McDonald, R., Goldschmidt, B.: Pancytopenia with congential defects (Fanconi's anaemia). Arch. Dis. Childh. 35, 367?372 (1960)
(
10.1136/adc.35.182.367
) / Arch. Dis. Childh. by R. McDonald (1960) - McDonald, R., Mibashan, R. S.: Prolonged remission in Fanconi type anaemia. Helv. paediat. Acta 23, 566?576 (1968) / Helv. paediat. Acta by R. McDonald (1968)
- McKusick, V. A.: Mendelian inheritance in man, 1st ed. Baltimore-London: Hopkins Press 1966 / Mendelian inheritance in man by V. A. McKusick (1966)
- Morton, N. E.: Genetic tests under incomplete ascertainment. Amer. J. hum. Genet. 11, 1?16 (1959) / Amer. J. hum. Genet. by N. E. Morton (1959)
- Nilsby, I.: Constitutional anemia with multiple malformations (Fanconi's syndrome). Acta paediat. 49, 462?463 (1960) / Acta paediat. by I. Nilsby (1960)
-
Nilsson, L. R.: Chronic pancytopenia with multiple congenital abnormalities (Fanconi's anemia). Acta paediat. 49, 518?529 (1960)
(
10.1111/j.1651-2227.1960.tb07767.x
) / Acta paediat. by L. R. Nilsson (1960) -
Perkins, J., Timson, J., Emery, A. E. H.: Clinical and chromosome studies in Fanconi's aplastic anaemia. J. med. Genet. 6, 28?33 (1969)
(
10.1136/jmg.6.1.28
) / J. med. Genet. by J. Perkins (1969) -
Prindull, G., Stubbe, P., Kratzer, W.: Fanconi's anemia. I. Case histories, clinical and laboratory findings in six affected siblings. Z. Kinderheilk. 120, 37?49 (1975)
(
10.1007/BF00443798
) / Z. Kinderheilk. by G. Prindull (1975) -
Reinhold, J. D. L., Neumark, E., Lightwood, R., Carter, C. O.: Familial hypoplastic anemia with congenital abnormalities (Fanconi's syndrome). Blood 7, 915?926 (1952)
(
10.1182/blood.V7.9.915.915
) / Blood by J. D. L. Reinhold (1952) -
Rohr, K.: Familial panmyelophthisis. Fanconi syndrome in adults. Blood 4, 130?141 (1949)
(
10.1182/blood.V4.2.130.130
) / Blood by K. Rohr (1949) - Schmid, W., Schärer, K., Baumann, Th., Fanconi, G.: Chromosomebrüchigkeit bei der familiären Panmyelopathie (Typus Fanconi). Schweiz. med. Wschr. 95, 1461?1464 (1965) / Schweiz. med. Wschr. by W. Schmid (1965)
- Schroeder, T. M.: Cytogenetische und cytologische Befunde bei enzymopenischen Panmyelopathien und Pancytopenien (Familiäre Panmyelopathie Typ Fanconi, Glutathionreduktasemangel-Anämie und megaloblastäre Vitamin B12-Mangel-Anämie). Humangenetik 2, 287?316 (1966a) / Humangenetik by T. M. Schroeder (1966)
- Schroeder, T. M.: Cytogenetischer Befund und Ätiologie bei Fanconi-Anämie. Ein Fall von Fanconi-Anämie ohne Hexokinasedefekt. Humangenetik 3, 76?81 (1966b) / Humangenetik by T. M. Schroeder (1966)
- Schroeder, T. M.: Genetische Faktoren der Krebsentstehung. Fortschr. Med. 90, 603?608 (1972) / Fortschr. Med. by T. M. Schroeder (1972)
- Schroeder, T. M., Anschütz, F., Knopp, A.: Spontane Chromosomenaberrationen bei familiärer Panmyelopathie. Humangenetik 1, 194?196 (1964) / Humangenetik by T. M. Schroeder (1964)
- Schroeder, T. M., Drings, P.: Verlaufsbeobachtung einer Fanconi-Anämie bei einem Erwachsenen. Verh. dtsch. Ges. inn. Med. 79, 477?481 (1973) / Verh. dtsch. Ges. inn. Med. by T. M. Schroeder (1973)
-
Schroeder, T. M., Drings, P., Beilner, P., Buchinger, G.: Clinical and cytogenetic observations during a six-year period in an adult with Fanconi's anemia. Blut (in press, 1976)
(
10.1007/BF00999858
) -
Schroeder, T. M., German, J.: Bloom's syndrome and Fanconi's anemia: Demonstration of two distinctive patterns of chromosome disruption and rearrangement. Humangenetik 25, 299?306 (1974)
(
10.1007/BF00336905
) / Humangenetik by T. M. Schroeder (1974) -
Schroeder, T. M., Kurth, R.: Analytical review. Spontaneous chromosomal breakage and high incidence of leukemia in inherited disease. Blood 37, 96?112 (1971)
(
10.1182/blood.V37.1.96.96
) / Blood by T. M. Schroeder (1971) - Schuler, D., Kiss, A., Fábián, F.: Chromosomal peculiarities and ?in vitro? examinations in Fanconi's anaemia. Humangenetik 7, 314?322 (1969) / Humangenetik by D. Schuler (1969)
-
Shahidi, N. T., Gerald, P. S., Diamond, L. K.: Alkali-resistant hemoglobin in aplastic anemia of both acquired and congenital types. New Engl. J. Med. 266, 117?120 (1962)
(
10.1056/NEJM196201182660303
) / New Engl. J. Med. by N. T. Shahidi (1962) - Silver, H. K., Blair, W. C., Kempe, C. H.: Fanconi syndrome. Amer. J. Dis. Child. 83, 14?25 (1952) / Amer. J. Dis. Child. by H. K. Silver (1952)
-
Sjölin, S., Wranne, L.: Erythropoietic dysfunction in a case of Fanconi's anaemia. Acta haemat. (Basel) 28, 230?238 (1962)
(
10.1159/000207276
) / Acta haemat. (Basel) by S. Sjölin (1962) -
Stevenson, A. C., Cheeseman, E. A.: Hereditary deafmutism with particular reference to Northern Ireland. Ann. hum. Genet. 20, 177?231 (1955/56)
(
10.1111/j.1469-1809.1956.tb01367.x
) / Ann. hum. Genet. by A. C. Stevenson (1955/56) -
Swift, M.: Fanconi's anaemia in the genetics of neoplasia. Nature (Lond.) 230, 370?373 (1971)
(
10.1038/230370a0
) / Nature (Lond.) by M. Swift (1971) -
Swift, M. R., Hirschhorn, K.: Fanconi's anemia. Inherited susceptibility to chromosome breakage in various tissues. Ann. intern. Med. 65, 496?503 (1966)
(
10.7326/0003-4819-65-3-496
) / Ann. intern. Med. by M. R. Swift (1966) -
Swift, M., Sholman, L., Gilmour, D.: Diabetes mellitus and the gene for Fanconi's anemia. Science 178, 308?310 (1972)
(
10.1126/science.178.4058.308
) / Science by M. Swift (1972) -
Swift, M., Zimmermann, D., McDonough, E. R.: Squamous cell carcinomas in Fanconi's anemia. J. Amer. med. Ass. 216, 325?326 (1971)
(
10.1001/jama.1971.03180280079018
) / J. Amer. med. Ass. by M. Swift (1971) -
Syllm-Rapoport, I., Gmyrek, D., Altenbrunn, H.-J., Scheuch, D., Jacobasch, G.: Studien zur Hämolyse bei der Fanconi-Anämie. Erhöhung der ATP-ase als eine mögliche Ursache erniedrigter ATP-Werte. Dtsch. med. Wschr. 90, 290?296 (1965)
(
10.1055/s-0028-1111334
) / Dtsch. med. Wschr. by I. Syllm-Rapoport (1965) - Tilgen, D.: Zur Genetik der Fanconi-Anämie (FA). Diss., Heidelberg 1975
-
Uehlinger, E.: Konstitutionelle infantile (perniciosaartige) Anämie. Klin. Wschr. 8, 1501?1503 (1929)
(
10.1007/BF01847068
) / Klin. Wschr. by E. Uehlinger (1929) - Vaccaro, R., Puxeddu, A., Brunetti, B.: Contributo allo studio dell'emolisi nell'anemia di Fanconi. Haematologica 51, 745?770 (1966) / Haematologica by R. Vaccaro (1966)
- Vogel, F.: Methoden zur Prüfung der Reihenfolge von Merkmalsträgern und Gesunden in Geschwisterschaften. Z. menschl. Vererb.-u. Konstit.-Lehre 34, 194?204 (1957) / Z. menschl. Vererb.-u. Konstit.-Lehre by F. Vogel (1957)
-
Vogel, F.: Lehrbuch der allgemeinen Humangenetik. Berlin-Göttingen-Heidelberg: Springer 1961
(
10.1007/978-3-642-87295-2
) / Lehrbuch der allgemeinen Humangenetik by F. Vogel (1961) - Weicker, H.: Die genetischen Grundlagen der Fanconi-Anämie. Schweiz. med. Wschr. 89, 1081?1082 (1959) / Schweiz. med. Wschr. by H. Weicker (1959)
-
Zaizov, R., Matoth, Y., Mamon, Z.: Familial aplastic anaemia without congenital malformations. Acta paediat. scand. 58, 151?156 (1969)
(
10.1111/j.1651-2227.1969.tb04699.x
) / Acta paediat. scand. by R. Zaizov (1969) - Zellweger, H., Zollinger, H. U.: Über einen sporadischen Fall von konstitutioneller, infantiler Panmyelopathie Fanconi. Helv. paediat. Acta 1, 382?394 (1946) / Helv. paediat. Acta by H. Zellweger (1946)
Dates
Type | When |
---|---|
Created | 20 years, 10 months ago (Oct. 20, 2004, 1:56 a.m.) |
Deposited | 1 year, 7 months ago (Jan. 14, 2024, 12:49 p.m.) |
Indexed | 10 hours, 24 minutes ago (Sept. 4, 2025, 9:12 a.m.) |
Issued | 49 years, 8 months ago (Jan. 1, 1976) |
Published | 49 years, 8 months ago (Jan. 1, 1976) |
Published Print | 49 years, 8 months ago (Jan. 1, 1976) |
@article{Schroeder_1976, title={Formal genetics of Fanconi’s anemia}, volume={32}, ISSN={1432-1203}, url={http://dx.doi.org/10.1007/bf00295817}, DOI={10.1007/bf00295817}, number={3}, journal={Human Genetics}, publisher={Springer Science and Business Media LLC}, author={Schroeder, T. M. and Tilgen, D. and Kr�ger, J. and Vogel, F.}, year={1976}, pages={257–288} }