Distal trisomy 14qMIKELSAAR, R. V.-A; ILUS, T. A; LURIE, I. W et al.Journal of medical genetics. 1987, Vol 24, Num 6, pp 380-381, issn 0022-2593Article

First case of deletion 14q11.2q13: clinical phenotypeGRAMMATICO, P; DE SANCTIS, S; DI ROSA, C et al.Annales de génétique (Paris). 1994, Vol 37, Num 1, pp 30-32, issn 0003-3995Article

Krabbe disease locus mapped to chromosome 14 by genetic linkageZLOTOGORA, J; CHAKRABORTY, S; KNOWLTON, R. G et al.American journal of human genetics. 1990, Vol 47, Num 1, pp 37-44, issn 0002-9297, 8 p.Article

Duplication 14(q31→qter)CARR, D. M; JONES-QUARTEY, K; VARTANIAN, M. V et al.Journal of medical genetics. 1987, Vol 24, Num 6, pp 372-374, issn 0022-2593Article

Unusual phenotype in partial trisomy 14LEMIRE, E. G; CARDWELL, S.American journal of medical genetics. 1999, Vol 87, Num 4, pp 294-296, issn 0148-7299Article

Unbalanced karyotype, dup 14(q13-q22), in a mother and her two childrenPOT, M. L. H; GILTAY, J. C; VAN WILSEN, A et al.Clinical genetics. 1996, Vol 50, Num 5, pp 398-402, issn 0009-9163Article

A variant t(14;17) in acute promyelocytic leukemia: positive response to retinoic acid treatmentCIGUDOSA, J. C; CALASANZ, M. J; ODERO, M. D et al.Cancer genetics and cytogenetics. 1995, Vol 80, Num 2, pp 160-161, issn 0165-4608Article

A further case of terminal deletion (14)(q32.2) in a child with mild dysmorphic featuresWANG, H. S; ALLANSON, J. E.Annales de génétique (Paris). 1992, Vol 35, Num 3, pp 171-173, issn 0003-3995Article

Opposite imbalances of distal 14q in two unrelated patientsRIVERA, H; RAMIREZ-DUENAS, M. L; FIGUERA, L. E et al.Annales de génétique (Paris). 1992, Vol 35, Num 2, pp 97-100, issn 0003-3995Article

The bcl-2 gene and protein in malignant lymphomasCLEARY, M. L.Bulletin du cancer. 1991, Vol 78, Num 2, pp 187-193, issn 0007-4551Article

Multiple levels of analysis of an IGHG4 gene deletionBOTTARO, A; CARIOTA, U; DE LANGE, G. G et al.Human genetics. 1990, Vol 86, Num 2, pp 191-197, issn 0340-6717Article

Transmission of ring 14 chromosome from mother to two sonsMATALON, R; SUPPLE, P; WYANDT, H et al.American journal of medical genetics. 1990, Vol 36, Num 4, pp 381-385, issn 0148-7299Article

Paracentric inversion 14MILLER, K; RAABE, G; SCHLESINGER, C et al.Annales de génétique (Paris). 1990, Vol 33, Num 4, pp 225-227, issn 0003-3995Article

Chromosome analysis of 30 cases of non-Hodgkin's lymphomaCHENEVIX-TRENCH, G; BROWN, J. A; TYLER, G. B et al.Medical oncology and tumor pharmacotherapy. 1988, Vol 5, Num 1, pp 17-32, issn 0736-0118Article

Correlation of secondary cytogenetic abnormalities with histologic appearance in non-Hodgkin's lymphomas bearing t(14;18) (q32;q21)ARMITAGE, J. O; SANGER, W. G; WEISENBURGER, D. D et al.Journal of the National Cancer Institute. 1988, Vol 80, Num 8, pp 576-580, issn 0027-8874Article

Trisomy 14 in refractory anemia with excess of blasts in transformationHAAS, O. A; JAGER, U; AMBROS, P et al.Cancer genetics and cytogenetics. 1987, Vol 29, Num 2, pp 315-318, issn 0165-4608Article

A case of perineal hypospadias with paracentric inversion of chromosome 14LEUNG, A. K. C; HOO, J. J.European journal of pediatrics. 1986, Vol 144, Num 5, pp 503-504, issn 0340-6199Article

Involvement of chromosomes 12 and 14 in the cutaneous stage of mycosis fungoides: cytogenetic evidence for a multistep pathogenesis of the diseaseBARBIERI, D; SPANEDDA, R; CASTOLDI, G. L et al.Cancer genetics and cytogenetics. 1986, Vol 20, Num 3-4, pp 287-292, issn 0165-4608Article

Deletions at 14q in malignant mesothelioma detected by microsatellite marker analysisBJÖRKQVIST, A.-M; WOLF, M; NORDLING, S et al.British journal of cancer. 1999, Vol 81, Num 7, pp 1111-1115, issn 0007-0920Article

Need for search for cryptic translocation in parents with several children affected with mca : Report of a cryptic translocation (10;14) detected by FISHDELNESTE, D; VAMOS, E; PIERQUIN, G et al.Genetic counseling. 1998, Vol 9, Num 2, pp 97-102, issn 1015-8146Conference Paper

Delineation of 14q32.3 deletion syndromeORTIGAS, A. P; STEIN, C. K; THOMSON, L. L et al.Journal of medical genetics. 1997, Vol 34, Num 6, pp 515-517, issn 0022-2593Article

Child with multiple congenital anomalies and mosaicism 46, XX/46,XX, del (14)(q32.3)MILLER, B. A; JAYAKAR, P; CAPO, H et al.American journal of medical genetics. 1992, Vol 44, Num 5, pp 635-637, issn 0148-7299Article

Deletion (14) (q24.3q32.1) : evidence for a distinct clinical phenotypeKARNITIS, S. A; BURNS, K; SUDDUTH, K. W et al.American journal of medical genetics. 1992, Vol 44, Num 2, pp 153-157, issn 0148-7299Article

Late separating D/D fusions in subjects with balanced translocationMEHES, K; BAJNOCZKY, K; BUÊHLER, E. M et al.Annales de génétique (Paris). 1991, Vol 34, Num 1, pp 19-21, issn 0003-3995, 3 p.Article

An unusual translocation 46,XX,t(14;17)(q33.2;p11.2) in a woman with recurrent spontaneous abortionsCALZOLARI, E; AZZINI, G; PALAZZI, P et al.Human genetics. 1985, Vol 71, Num 2, issn 0340-6717, 181Article