FANCONI'S ANAEMIA: RECENT ADVANCES IN DIAGNOSIS AND TREATMENT = ANEMIE DE FANCONI: ACQUISITIONS RECENTES DANS LE DIAGNOSTIC ET LE TRAITEMENTBEARD MEJ.1972; PROC. R. SOC. MED.; G.B.; DA. 1972; VOL. 65; NO 9; PP. 747-748; BIBL. 8 REF.Serial Issue

DIABETES MELLITUS AND THE GENE FOR FANCONI'S ANEMIA = DIABETE SUCRE ET GENE POUR L'ANEMIE DE FANCONISWIFT M; SHOLMAN L; GILMOUR D et al.1972; SCIENCE; U.S.A.; DA. 1972; VOL. 178; NO 4058; PP. 308-310; BIBL. 13REF.Serial Issue

RED CELL DEFECT, IN FANCONI'S ANEMIA = DEFAUTS DES HEMATIES DANS L'ANEMIE DE FANCONIPOCHEDLY C; VERNICK S; COLLIP PJ et al.1972; MOUNT SINAI J. MED.; U.S.A.; DA. 1972; VOL. 39; NO 6; PP. 592-597; BIBL. 17REF.Serial Issue

SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtypeSTOEPKER, Chantal; HAIN, Karolina; JASPERS, Nicolaas G. J et al.Nature genetics. 2011, Vol 43, Num 2, pp 138-141, issn 1061-4036, 4 p.Article

HES1 is a novel interactor of the Fanconi anemia core complexTREMBLAY, Cédric S; HUANG, Feng F; HABI, Ouassila et al.Blood. 2008, Vol 112, Num 5, pp 2062-2070, issn 0006-4971, 9 p.Article

Fanconi AnemiaGREEN, Allison M; KUPFER, Gary M.Hematology/oncology clinics of North America. 2009, Vol 23, Num 2, issn 0889-8588, vii-viii, 193-214 [23 p.]Article

On the role of FAN1 in Fanconi anemiaTRUJILLO, Juan P; MINA, Leonardo B; PUJOL, Roser et al.Blood. 2012, Vol 120, Num 1, pp 86-89, issn 0006-4971, 4 p.Article

Fanconi AnemiaSALINAS, Alfredo; ESCAMILLA, Cesar; RIVERA, Gerardo et al.Archives of pediatrics & adolescent medicine. 2012, Vol 166, Num 7, pp 657-658, issn 1072-4710, 2 p.Article

Mutations of the SLX4 gene in Fanconi anemiaKIM, Yonghwan; LACH, Francis P; DESETTY, Rohini et al.Nature genetics. 2011, Vol 43, Num 2, pp 142-146, issn 1061-4036, 5 p.Article

ZUR PANMYELOPATHIE IM KINDESALTER = SUR LA PANMYELOPATHIE CHEZ L'ENFANTGOETZ M; PICHLER E.1972; KLIN. PAEDIATR.; DTSCH.; DA. 1972; VOL. 184; NO 5; PP. 377-384; ABS. ANGL.; BIBL. 28REF.Serial Issue

CYTOGENETIC FINDINGS IN A PARENT OF A PATIENT WITH FANCONI'S ANEMIA = CONSTATATIONS CYTOGENETIQUES CHEZ UN PARENT D'UN MALADE ATTEINT D'ANEMIE DE FANCONILIEBER E; HSU L; SPITTLER L et al.1972; CLIN. GENET.; DANM.; DA. 1972; VOL. 3; NO 5; PP. 357-363; BIBL. 24REF.Serial Issue

FANCONI'S ANAEMIA: REPORT OF A PATIENT WITH SIGNIFICANT CHROMOSOMAL ABNORMALITIES IN BONE MARROW CELLS = ANEMIE DE FANCONI: OBSERVATION D'UN MALADE PORTEUR D'ANOMALIES CHROMOSOMIQUES SIGNIFICATIVES AU NIVEAU DES CELLULES DE LA MOELLE OSSEUSESHAHID MJ; KHOURI FP; BALLAS SK et al.1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 4; PP. 474-478; BIBL. 10REF.Serial Issue

BONE MARROW CHROMOSOMES IN FANCONI'S ANAEMIA = LES CHROMOSOMES DE LA MOELLE OSSEUSE DANS L'ANEMIE DE FANCONIWOLMAN SR; SWIFT M.1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 4; PP. 473-474; BIBL. 6REF.Serial Issue

FANCONI'S ANEMIA IN A NEONATE = ANEMIE DE FANCONI CHEZ UN NOUVEAU-NEGERSHANIK JJ; MORGAN SK; AKERS R et al.1972; ACTA PAEDIATR. SCAND.; SUEDE; DA. 1972; VOL. 61; NO 5; PP. 623-625; BIBL. 12REF.Serial Issue

DISORDERS OF BONE MARROW PRODUCTION = LES TROUBLES DE LA PRODUCTION DE LA MOELLE OSSEUSEBLOOM GE.1972; PEDIATR. CLIN. N. AMER.; U.S.A.; DA. 1972; VOL. 19; NO 4; PP. 983-1008; BIBL. 6 P.Serial Issue

Déficit en GH par interruption de la tige pituitaire dans l'anémie de Fanconi = Growth hormone deficiency and pituitary stalk interruption in Fanconi anemiaLAMINE, F; TURKI, Z; MRAD, R et al.Annales d'endocrinologie. 2008, Vol 69, Num 1, pp 63-68, issn 0003-4266, 6 p.Article

FANCONI ANEMIA COMPLICATED BY NEUTROPENIC ENTEROCOLITISTINSA, Faten; NECIB, Nesrine; GUESMI, Manef et al.Tunisie médicale. 2008, Vol 86, Num 11, pp 1011-1013, issn 0041-4131, 3 p.Article

Pollicization of the index finger in Fanconi anaemia: appearances and functionality 40 years after the interventionSTIVAROS, Stavros M; PUNEKAR, Maqsood; CHANDLER, Kate et al.British journal of haematology. 2014, Vol 166, Num 6, issn 0007-1048, p. 807Article

The nuclease hSNM1B/Apollo is linked to the Fanconi anemia pathway via its interaction with FANCP/SLX4SALEWSKY, Bastian; SCHMIESTER, Maren; SCHINDLER, Detlev et al.Human molecular genetics (Print). 2012, Vol 21, Num 22, pp 4948-4956, issn 0964-6906, 9 p.Article

Snm1B/Apollo functions in the Fanconi anemia pathway in response to DNA interstrand crosslinksMASON, Jennifer M; SEKIGUCHI, Joann M.Human molecular genetics (Print). 2011, Vol 20, Num 13, pp 2549-2559, issn 0964-6906, 11 p.Article

Structure of the FANCI-FANCD2 Complex: Insights into the Fanconi Anemia DNA Repair PathwayJOO, Woo; GUOZHOU XU; PERSKY, Nicole S et al.Science (Washington, D.C.). 2011, Vol 333, Num 6040, pp 312-316, issn 0036-8075, 5 p.Article

PALB2/FANCN: Recombining Cancer and Fanconi AnemiaTISCHKOWITZ, Marc; BING XIA.Cancer research (Chicago, Ill.). 2010, Vol 70, Num 19, pp 7353-7359, issn 0008-5472, 7 p.Article

DNA damage and repair of leukocytes from Fanconi anaemia patients, carriers and healthy individuals as measured by the alkaline comet assayMOHSENI-MEYBODI, Anahita; MOZDARANI, Hossein; MOZDARANI, Sohail et al.Mutagenesis. 2009, Vol 24, Num 1, pp 67-73, issn 0267-8357, 7 p.Article

Fancm-deficient mice reveal unique features of Fanconi anemia complementation group MBAKKER, Sietske T; VAN DE VRUGT, Henri J; DE WINTER, Johan P et al.Human molecular genetics (Print). 2009, Vol 18, Num 18, pp 3484-3495, issn 0964-6906, 12 p.Article

Fanconi's Anemia in Monozygotic TwinsD' SOUZA, Fulton; USHA, M. K; SUBBA RAO, S. D et al.Indian journal of pediatrics. 2007, Vol 74, Num 9, pp 859-861, issn 0019-5456, 3 p.Article