-
1
-
-
33847300839
-
The Child Behavior Checklist/4-18. Washington, DC
-
ACHENBACH, T.M.: The Child Behavior Checklist/4-18. Washington, DC, Library of Congress, 1991.
-
(1991)
Library of Congress
-
-
ACHENBACH, T.M.1
-
2
-
-
0033615674
-
-
ANGELONI D., LINDOR N.M., PACK S., LATIF F., WEI M.H., LERMAN M.I.: CALL gene is haploinsufficient in a 3p- syndrome patient. Am. J. Med. Genet., 1999, 86, 482-485.
-
ANGELONI D., LINDOR N.M., PACK S., LATIF F., WEI M.H., LERMAN M.I.: CALL gene is haploinsufficient in a 3p- syndrome patient. Am. J. Med. Genet., 1999, 86, 482-485.
-
-
-
-
3
-
-
23744487028
-
Directly transmitted unbalanced chromosome abnormalities and euchromatic variants
-
BARBER J.C.K.: Directly transmitted unbalanced chromosome abnormalities and euchromatic variants. J. Med. Genet., 2005, 42, 609-629.
-
(2005)
J. Med. Genet
, vol.42
, pp. 609-629
-
-
BARBER, J.C.K.1
-
4
-
-
0037156322
-
Molecular cytogenetic characterization of a subtle del(3)(p25.3p26.2) in a patient with deletion 3p syndrome
-
CARGILE C.B., GOH D.L., GOODMAN B.K., CHEN X.N., KORENBERG J.R., SEMENZA G.L., THOMAS G.H.: Molecular cytogenetic characterization of a subtle del(3)(p25.3p26.2) in a patient with deletion 3p syndrome. Am. J. Med. Genet., 2002, 109, 133-138.
-
(2002)
Am. J. Med. Genet
, vol.109
, pp. 133-138
-
-
CARGILE, C.B.1
GOH, D.L.2
GOODMAN, B.K.3
CHEN, X.N.4
KORENBERG, J.R.5
SEMENZA, G.L.6
THOMAS, G.H.7
-
5
-
-
0036357205
-
Behavioral phenotypes in genetic syndromes: Genetic clues to human behavior
-
CASSIDY S.B., MORRIS C.A.: Behavioral phenotypes in genetic syndromes: genetic clues to human behavior. Adv. Pediatr., 2002, 49, 59-86.
-
(2002)
Adv. Pediatr
, vol.49
, pp. 59-86
-
-
CASSIDY, S.B.1
MORRIS, C.A.2
-
6
-
-
0033852945
-
Detailed mapping of a congenital heart disease gene in chromosome 3p25
-
GREEN E.K., PRIESTLEY M.D, WATERS J., MALISZEWSKA C., LATIF F., MAHER E.R.: Detailed mapping of a congenital heart disease gene in chromosome 3p25. J. Med. Genet., 2000, 37, 581-587.
-
(2000)
J. Med. Genet
, vol.37
, pp. 581-587
-
-
GREEN, E.K.1
PRIESTLEY, M.D.2
WATERS, J.3
MALISZEWSKA, C.4
LATIF, F.5
MAHER, E.R.6
-
7
-
-
2442641704
-
Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome
-
FERNANDEZ T., MORGAN T., DAVIS N., KLIN A., MORRIS A., FARHI A., LIFTON R.P., STATE M.W.: Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome. Am. J. Hum. Genet., 2004, 74, 1286-1293.
-
(2004)
Am. J. Hum. Genet
, vol.74
, pp. 1286-1293
-
-
FERNANDEZ, T.1
MORGAN, T.2
DAVIS, N.3
KLIN, A.4
MORRIS, A.5
FARHI, A.6
LIFTON, R.P.7
STATE, M.W.8
-
8
-
-
10744233700
-
CALL interrupted in a patient with non-specific mental retardation: Gene dosage-dependent alteration of murine brain development and behavior
-
FRINTS S.G., MARYNEN P., HARTMANN D., FRYNS J.P., STEYAERT J., SCHACHNER M., ROLF B., CRAESSAERTS K., SNELLINX A., HOLLANDERS J., D'HOGE R., DE DEYN P.P., FROYEN G.: CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behavior. Hum. Mol. Genet., 2003, 12, 1463-1474.
-
(2003)
Hum. Mol. Genet
, vol.12
, pp. 1463-1474
-
-
FRINTS, S.G.1
MARYNEN, P.2
HARTMANN, D.3
FRYNS, J.P.4
STEYAERT, J.5
SCHACHNER, M.6
ROLF, B.7
CRAESSAERTS, K.8
SNELLINX, A.9
HOLLANDERS, J.10
D'HOGE, R.11
DE DEYN, P.P.12
FROYEN, G.13
-
9
-
-
2942717198
-
Candidate genes for recessive non-syndromic mental retardation on chromosome 3p (MRTA2A)
-
HIGGINS J.J., PUCILOWSKA J., LOMBARDI R.Q., ROONEY J.P.: Candidate genes for recessive non-syndromic mental retardation on chromosome 3p (MRTA2A). Clin. Genet., 2004, 65, 496-500.
-
(2004)
Clin. Genet
, vol.65
, pp. 496-500
-
-
HIGGINS, J.J.1
PUCILOWSKA, J.2
LOMBARDI, R.Q.3
ROONEY, J.P.4
-
10
-
-
0028846586
-
del(3)(p25.3) without phenotypic effect
-
MIGHT L.A., YONG M.H., TAN M., NG I.S.L.: del(3)(p25.3) without phenotypic effect. J. Med. Genet., 1995, 32, 994-995.
-
(1995)
J. Med. Genet
, vol.32
, pp. 994-995
-
-
MIGHT, L.A.1
YONG, M.H.2
TAN, M.3
NG, I.S.L.4
-
11
-
-
33847318545
-
Deleción 3p26. Presentación de un nuevo caso
-
México, November 18-21
-
LIZCANO L.A., RIVERA H., FIGUERA L.E., DOMÍNGUEZ M.G.: Deleción 3p26. Presentación de un nuevo caso. In: Memorias del XVII Congreso Nacional de Genética Humana. Mazatlán, México, November 18-21, 1992, p. 48.
-
(1992)
Memorias del XVII Congreso Nacional de Genética Humana. Mazatlán
, pp. 48
-
-
LIZCANO, L.A.1
RIVERA, H.2
FIGUERA, L.E.3
DOMÍNGUEZ, M.G.4
-
12
-
-
0028220413
-
Terminal deletion of the short arm of chromosome 3
-
LIZCANO-GIL L.A., FIGUERA L.E.: Terminal deletion of the short arm of chromosome 3. Genet. Counsel., 1994, 5, 35-38.
-
(1994)
Genet. Counsel
, vol.5
, pp. 35-38
-
-
LIZCANO-GIL, L.A.1
FIGUERA, L.E.2
-
13
-
-
33847336302
-
-
nd ed. London, BMJ Publishing Group, 1996.
-
nd ed. London, BMJ Publishing Group, 1996.
-
-
-
-
14
-
-
33847295550
-
-
MARTINEZ M., ZENTENO-SAVIN T.: El papel y estructura de una comisión de ética en una institución académica. In: El Papel de la Ética en la Investigación Científica y la Educación Superior. M. Aluja, A. Birke (eds). México City, Academia Mexicana de Ciencias, 2003, 167-174.
-
MARTINEZ M., ZENTENO-SAVIN T.: El papel y estructura de una comisión de ética en una institución académica. In: El Papel de la Ética en la Investigación Científica y la Educación Superior. M. Aluja, A. Birke (eds). México City, Academia Mexicana de Ciencias, 2003, 167-174.
-
-
-
-
15
-
-
33847263352
-
Evaluación Neuropsicológica Infantil - ENI. Manual Moderno. UNAM, UdeG, México
-
in press
-
MATUTE E., ROSSELLI M., ARDILA A., OSTROSKY F.: Evaluación Neuropsicológica Infantil - ENI. Manual Moderno. UNAM, UdeG, México, 2006, in press.
-
(2006)
-
-
MATUTE, E.1
ROSSELLI, M.2
ARDILA, A.3
OSTROSKY, F.4
-
16
-
-
0030337626
-
Fragile X studies and authorship
-
RIVERA H.: Fragile X studies and authorship. Arch. Med. Res., 1996, 27, 587-588.
-
(1996)
Arch. Med. Res
, vol.27
, pp. 587-588
-
-
RIVERA, H.1
-
18
-
-
33745622176
-
Chromosome 3p25 deletion in mother and daughter with minimal phenotypic effect
-
TAKAGISHI J., RAUEN K.A., DRUMHELLER T., KOUSSEFF B., SUTCLIFFE M.: Chromosome 3p25 deletion in mother and daughter with minimal phenotypic effect. Am. J. Med. Genet. A, 2006, 140, 1587-1593.
-
(2006)
Am. J. Med. Genet. A
, vol.140
, pp. 1587-1593
-
-
TAKAGISHI, J.1
RAUEN, K.A.2
DRUMHELLER, T.3
KOUSSEFF, B.4
SUTCLIFFE, M.5
|