Assignment¹ of the Aquaporin-8 water channel gene (AQP8) to human chromosome 16p12VIGGIANO, L; ROCCHI, M; SVELTO, M et al.Cytogenetics and cell genetics. 1999, Vol 84, Num 3-4, pp 208-210, issn 0301-0171Article

Assignment^a of the human creatine transporter type 2(SLC6A10) to chromosome band 16p11.2 by in situ hybridizationXU, W; LIU, L; GORMAN, P. A et al.Cytogenetics and cell genetics. 1997, Vol 76, Num 1-2, issn 0301-0171, p. 19Article

Homozygous Structural Rearrangement 16p13 : A Mechanism of Tumorigenesis in Sporadic Renal Angiomyolipoma?ADEYINKA, Adewale; SAINAN WEI; ABBUD-MENDEZ, Cesar et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 4, pp 809-811, issn 1552-4825, 3 p.Article

Trisomy 16p : A longitudinal profile and photo essaySOMMER, Annemarie; PASTORE, Matthew; WENGER, Gail et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 2, pp 174-179, issn 1552-4825, 6 p.Article

The sequence and analysis of duplication-rich human chromosome 16MARTIN, Joel; HAN, Cliff; COURONNE, Olivier et al.Nature (London). 2004, Vol 432, Num 7020, pp 988-994, issn 0028-0836, 7 p.Article

Assignment of the E-cadherin gene (CDH 1) to chromosome 16q22.1 by radiation hybrid mappingHUNTSMAN, D. G; CALDAS, C.Cytogenetics and cell genetics. 1998, Vol 83, Num 1-2, pp 82-83, issn 0301-0171Article

Non-mosaic trisomy 16 16 in a third-trimester fetusYANCEY, M. K; HARDIN, E. L; PACHECO, C et al.Obstetrics and gynecology (New York. 1953). 1996, Vol 87, Num 5, pp 856-860, issn 0029-7844, 2Article

FREQUENCY AND SEGREGATION OF 16 QH+ = FREQUENCE ET SEGREGATION DE 16 QH+NIELSEN J; FRIEDRICH U; HREIDARSSON AB et al.1974; CLIN. GENET.; DANM.; DA. 1974; VOL. 5; NO 4; PP. 316-321; BIBL. 9REF.Article

TRISOMY OF CHROMOSOME 16 IN A NEONATE, 47,XY,.16+ = TRISOMIE DU CHROMOSOME 16 CHEZ UN NOUVEAU-NE 47,XY,.16+TAYLOR AI.1971; J. MED. GENET.; G.B.; DA. 1971; VOL. 8; NO 1; PP. 123-125; BIBL. 4REF.Serial Issue

Association study of autistic disorder and chromosome 16pLUCARELLI, Paola; PALMINIELLO, Sonia; SACCUCCI, Patrizia et al.American journal of medical genetics. 2003, Vol 119A, Num 2, pp 242-246, issn 0148-7299, 5 p.Article

Regional mapping panels for chromosomes 6, 9, and 16LEONARD, J. C; TOJI, L. H; BENDER, P. K et al.Genomics (San Diego, Calif.). 1999, Vol 58, Num 3, pp 323-326, issn 0888-7543Article

International Workshop on Human Chromosome 16 Mapping 1995Cytogenetics and cell genetics. 1996, Vol 72, Num 4, pp 271-293, issn 0301-0171Conference Proceedings

Integrated analysis of sequence evolution and population history using hypervariable compound haplotypesROGERS, Emma J; SHONE, Angela C; ALONSO, Santos et al.Human molecular genetics (Print). 2000, Vol 9, Num 18, pp 2675-2681, issn 0964-6906Article

Assignment of herpesvirus-associated ubiquitin-specific protease gene HAUSP to human chromosome band 16p13.3 by in situ hybridizationROBINSON, P. A; LOMONTE, P; LEEK, J. P et al.Cytogenetics and cell genetics. 1998, Vol 83, Num 1-2, issn 0301-0171, p. 100Article

Assignment of the gene for a ubiquitin-conjugating enzyme (UBE2I) to human chromosome band 16p13.3 by in situ hybridizationTACHIBANA, M; IWATA, N; WATANABE, A et al.Cytogenetics and cell genetics. 1996, Vol 75, Num 4, pp 222-223, issn 0301-0171Article

Benign chronic neutropenia with abnormalities involving 16q22, affecting mother and daughterGLASSER, Lewis; MELONI-EHRIG, Aurelia; JOSEPH, Plakyil et al.American journal of hematology. 2006, Vol 81, Num 4, pp 262-270, issn 0361-8609, 9 p.Article

From chromosomes to molecular karyotyping : Small reciprocal insertion detected by spectral karyotyping (SKY) and delimited by array-CGH analysisMATTHAEI, Anja; WEMER, Walter; SCHROCK, Evelin et al.European journal of medical genetics. 2005, Vol 48, Num 3, pp 328-338, issn 1769-7212, 11 p.Article

Five-color-based high-information-content fingerprinting of bacterial artificial chromosome clones using Type IIS restriction endonucleasesDING, Y; JOHNSON, M. D; CHEN, W. Q et al.Genomics (San Diego, Calif.). 2001, Vol 74, Num 2, pp 142-154, issn 0888-7543Article

Assignment¹ of TRADD to human chromosome band 16q22 by in situ hybridizationSCHEUERPFLUG, C. G; LICHTER, P; DEBATIN, K.-M et al.Cytogenetics and cell genetics. 2001, Vol 92, Num 3-4, pp 347-348, issn 0301-0171Article

Human chemokines fractalkine (SCYD1), MDC (SCYA22) and TARC (SCYA17) are clustered on chromosome 16q13NOMIYAMA, H; IMAI, T; KUSUDA, J et al.Cytogenetics and cell genetics. 1998, Vol 81, Num 1, pp 10-11, issn 0301-0171Article

Assignment of the human CC chemokine gene TARC (SCYA17) to chromosome 16q13NOMIYAMA, H; IMAI, T; KUSUDA, J et al.Genomics (San Diego, Calif.). 1997, Vol 40, Num 1, pp 211-213, issn 0888-7543Article

Variant euchromatic band within 16q12.1VERMA, R. S; KLEYMAN, S. M; CONTE, R. A et al.Clinical genetics. 1997, Vol 52, Num 6, pp 446-447, issn 0009-9163Article

Assignment of the human syntaxin 1B gene (STX) to chromosome 16p11.2 by fluorescence in situ hybridizationSMIRNOVA, T; MINIOU, P; VIEGAS-PEQUIGNOT, E et al.Genomics (San Diego, Calif.). 1996, Vol 36, Num 3, pp 551-553, issn 0888-7543Article

A molecular anatomical analysis of mosaic trisomy 16GREALLY, J. M; NEISWANGER, K; CUMMINS, J. H et al.Human genetics. 1996, Vol 98, Num 1, pp 86-90, issn 0340-6717Article

A new familial «fragile site» on chromosome 16 (q23-24). Cytogenetic and clinical considerationsSHABTAI, F; KLAR, D; NISSIMOV, R et al.Human genetics. 1983, Vol 64, Num 3, pp 273-276, issn 0340-6717Article