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Level of functioning of siblings and parents of probands of varying degrees of retardation.

Behavior genetics

Johnson CA, Ahern FM, Johnson RC.
PMID: 988824
Behav Genet. 1976 Oct;6(4):473-7. doi: 10.1007/BF01065704.

A further analysis of already published data supports the position that retardates of low ability level less frequently have retarded siblings, retarded parents, and parents low in occupational level than do retardates higher in ability level. The analysis supports...

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Johnson CA, Ahern FM, Johnson RC. Level of functioning of siblings and parents of probands of varying degrees of retardation. Behav Genet. 1976;6(4):473-7doi: 10.1007/BF01065704.
Johnson, C. A., Ahern, F. M., & Johnson, R. C. (1976). Level of functioning of siblings and parents of probands of varying degrees of retardation. Behavior genetics, 6(4), 473-7. https://doi.org/10.1007/BF01065704
Johnson, C A, et al. "Level of functioning of siblings and parents of probands of varying degrees of retardation." Behavior genetics vol. 6,4 (1976): 473-7. doi: https://doi.org/10.1007/BF01065704
Johnson CA, Ahern FM, Johnson RC. Level of functioning of siblings and parents of probands of varying degrees of retardation. Behav Genet. 1976 Oct;6(4):473-7. doi: 10.1007/BF01065704. PMID: 988824.
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[Clinico-cytogenetic correlates in oligophrenias].

Revista espanola de oto-neuro-oftalmologia y neurocirugia

Amat Aguirre E, Barcia Salorio D.
PMID: 5826807
Rev Esp Otoneurooftalmol Neurocir. 1965 Mar-Apr;24(138):85-101.

No abstract available.

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Amat Aguirre E, Barcia Salorio D. Correlación clinicocitogenética en las oligofrenias. [Clinico-cytogenetic correlates in oligophrenias]. Rev Esp Otoneurooftalmol Neurocir. 1965;24(138):85-101
Amat Aguirre, E., & Barcia Salorio, D. (1965). Correlación clinicocitogenética en las oligofrenias. [Clinico-cytogenetic correlates in oligophrenias]. Revista espanola de oto-neuro-oftalmologia y neurocirugia, 24(138), 85-101.
Amat Aguirre, E, and Barcia Salorio, D. "Correlación clinicocitogenética en las oligofrenias." [Clinico-cytogenetic correlates in oligophrenias]. Revista espanola de oto-neuro-oftalmologia y neurocirugia vol. 24,138 (1965): 85-101.
Amat Aguirre E, Barcia Salorio D. Correlación clinicocitogenética en las oligofrenias. [Clinico-cytogenetic correlates in oligophrenias]. Rev Esp Otoneurooftalmol Neurocir. 1965 Mar-Apr;24(138):85-101. Spanish. PMID: 5826807.
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[Oligophrenia].

Pediatria

Maximilian C.
PMID: 5593251
Pediatria (Bucur). 1967 Jul-Aug;16(4):374-6.

No abstract available.

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Maximilian C. Oligofrenia. [Oligophrenia]. Pediatria (Bucur). 1967;16(4):374-6
Maximilian, C. (1967). Oligofrenia. [Oligophrenia]. Pediatria, 16(4), 374-6.
Maximilian, C. "Oligofrenia." [Oligophrenia]. Pediatria vol. 16,4 (1967): 374-6.
Maximilian C. Oligofrenia. [Oligophrenia]. Pediatria (Bucur). 1967 Jul-Aug;16(4):374-6. Romanian. PMID: 5593251.
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[Mental retardation. Progress in the search of causes means new challenge for the clinician].

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke

Orstavik KH.
PMID: 9198916
Tidsskr Nor Laegeforen. 1997 Apr 20;117(10):1438.

No abstract available.

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Orstavik KH. Psykisk utviklingshemning. Fremskritt i jakten på årsaker gir nye utfordringer for den behandlende lege. [Mental retardation. Progress in the search of causes means new challenge for the clinician]. Tidsskr Nor Laegeforen. 1997;117(10):1438
Orstavik, K. H. (1997). Psykisk utviklingshemning. Fremskritt i jakten på årsaker gir nye utfordringer for den behandlende lege. [Mental retardation. Progress in the search of causes means new challenge for the clinician]. Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 117(10), 1438.
Orstavik, K H. "Psykisk utviklingshemning. Fremskritt i jakten på årsaker gir nye utfordringer for den behandlende lege." [Mental retardation. Progress in the search of causes means new challenge for the clinician]. Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke vol. 117,10 (1997): 1438.
Orstavik KH. Psykisk utviklingshemning. Fremskritt i jakten på årsaker gir nye utfordringer for den behandlende lege. [Mental retardation. Progress in the search of causes means new challenge for the clinician]. Tidsskr Nor Laegeforen. 1997 Apr 20;117(10):1438. Norwegian. PMID: 9198916.
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Genetic factors in the etiology of mental retardation.

International record of medicine and general practice clinics

GOODMAN HO, HERNDON CN.
PMID: 13620361
Int Rec Med Gen Pract Clin. 1959 Feb;172(2):61-74.

No abstract available.

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GOODMAN HO, HERNDON CN. Genetic factors in the etiology of mental retardation. Int Rec Med Gen Pract Clin. 1959;172(2):61-74
GOODMAN, H. O., & HERNDON, C. N. (1959). Genetic factors in the etiology of mental retardation. International record of medicine and general practice clinics, 172(2), 61-74.
GOODMAN, H O, and HERNDON, C N. "Genetic factors in the etiology of mental retardation." International record of medicine and general practice clinics vol. 172,2 (1959): 61-74.
GOODMAN HO, HERNDON CN. Genetic factors in the etiology of mental retardation. Int Rec Med Gen Pract Clin. 1959 Feb;172(2):61-74. PMID: 13620361.
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The Vale of Siddem revisited.

American journal of mental deficiency

REED EW, PHILLIPS VP.
PMID: 13617309
Am J Ment Defic. 1959 Jan;63(4):699-702.

No abstract available.

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REED EW, PHILLIPS VP. The Vale of Siddem revisited. Am J Ment Defic. 1959;63(4):699-702
REED, E. W., & PHILLIPS, V. P. (1959). The Vale of Siddem revisited. American journal of mental deficiency, 63(4), 699-702.
REED, E W, and PHILLIPS, V P. "The Vale of Siddem revisited." American journal of mental deficiency vol. 63,4 (1959): 699-702.
REED EW, PHILLIPS VP. The Vale of Siddem revisited. Am J Ment Defic. 1959 Jan;63(4):699-702. PMID: 13617309.
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Phylogenetic evolutionary deviation and deviation in a child.

Annales medico-psychologiques

ABELY X, MARTY, LUQUET.
PMID: 20990279
Ann Med Psychol (Paris). 1946 May;104:446-8.

No abstract available.

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ABELY X, MARTY, LUQUET. Arriération et déviation évolutive phylogéniques chez un enfant. Phylogenetic evolutionary deviation and deviation in a child. Ann Med Psychol (Paris). 1946;104:446-8
ABELY, X., MARTY, & LUQUET. (1946). Arriération et déviation évolutive phylogéniques chez un enfant. Phylogenetic evolutionary deviation and deviation in a child. Annales medico-psychologiques, 104446-8.
ABELY, X, et al. "Arriération et déviation évolutive phylogéniques chez un enfant." Phylogenetic evolutionary deviation and deviation in a child. Annales medico-psychologiques vol. 104 (1946): 446-8.
ABELY X, MARTY, LUQUET. Arriération et déviation évolutive phylogéniques chez un enfant. Phylogenetic evolutionary deviation and deviation in a child. Ann Med Psychol (Paris). 1946 May;104:446-8. French. PMID: 20990279.
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"You have to sit and explain it all, and explain yourself." Mothers' experiences of support services for their offspring with a rare genetic intellectual disability syndrome.

Journal of genetic counseling

Griffith GM, Hastings RP, Nash S, Petalas M, Oliver C, Howlin P, Moss J, Petty J, Tunnicliffe P.
PMID: 21203808
J Genet Couns. 2011 Apr;20(2):165-77. doi: 10.1007/s10897-010-9339-4. Epub 2011 Jan 04.

The experiences of mothers of adult offspring with Angelman, Cornelia de Lange, or Cri du Chat syndrome have not been previously explored in research. The current study focuses on experiences with social and medical services and the impact the...

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Griffith GM, Hastings RP, Nash S, et al. "You have to sit and explain it all, and explain yourself." Mothers' experiences of support services for their offspring with a rare genetic intellectual disability syndrome. J Genet Couns. 2011;20(2):165-77doi: 10.1007/s10897-010-9339-4.
Griffith, G. M., Hastings, R. P., Nash, S., Petalas, M., Oliver, C., Howlin, P., Moss, J., Petty, J., & Tunnicliffe, P. (2011). "You have to sit and explain it all, and explain yourself." Mothers' experiences of support services for their offspring with a rare genetic intellectual disability syndrome. Journal of genetic counseling, 20(2), 165-77. https://doi.org/10.1007/s10897-010-9339-4
Griffith, Gemma Maria, et al. ""You have to sit and explain it all, and explain yourself." Mothers' experiences of support services for their offspring with a rare genetic intellectual disability syndrome." Journal of genetic counseling vol. 20,2 (2011): 165-77. doi: https://doi.org/10.1007/s10897-010-9339-4
Griffith GM, Hastings RP, Nash S, Petalas M, Oliver C, Howlin P, Moss J, Petty J, Tunnicliffe P. "You have to sit and explain it all, and explain yourself." Mothers' experiences of support services for their offspring with a rare genetic intellectual disability syndrome. J Genet Couns. 2011 Apr;20(2):165-77. doi: 10.1007/s10897-010-9339-4. Epub 2011 Jan 04. PMID: 21203808.
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[Exomes, again: de novo mutations in mental retardation].

Medecine sciences : M/S

Jordan B.
PMID: 21382334
Med Sci (Paris). 2011 Feb;27(2):220-2. doi: 10.1051/medsci/2011272220. Epub 2011 Mar 08.

No abstract available.

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Jordan B. Exomes, le retour… Exomes et mutations de novo dans le retard mental - Chroniques génomiques. [Exomes, again: de novo mutations in mental retardation]. Med Sci (Paris). 2011;27(2):220-2doi: 10.1051/medsci/2011272220.
Jordan, B. (2011). Exomes, le retour… Exomes et mutations de novo dans le retard mental - Chroniques génomiques. [Exomes, again: de novo mutations in mental retardation]. Medecine sciences : M/S, 27(2), 220-2. https://doi.org/10.1051/medsci/2011272220
Jordan, Bertrand. "Exomes, le retour… Exomes et mutations de novo dans le retard mental - Chroniques génomiques." [Exomes, again: de novo mutations in mental retardation]. Medecine sciences : M/S vol. 27,2 (2011): 220-2. doi: https://doi.org/10.1051/medsci/2011272220
Jordan B. Exomes, le retour… Exomes et mutations de novo dans le retard mental - Chroniques génomiques. [Exomes, again: de novo mutations in mental retardation]. Med Sci (Paris). 2011 Feb;27(2):220-2. doi: 10.1051/medsci/2011272220. Epub 2011 Mar 08. French. PMID: 21382334.
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Distribution of disease-associated copy number variants across distinct disorders of cognitive development.

Journal of the American Academy of Child and Adolescent Psychiatry

Pescosolido MF, Gamsiz ED, Nagpal S, Morrow EM.
PMID: 23582872
J Am Acad Child Adolesc Psychiatry. 2013 Apr;52(4):414-430.e14. doi: 10.1016/j.jaac.2013.01.003.

OBJECTIVE: The purpose of the present study was to discover the extent to which distinct DSM disorders share large, highly recurrent copy number variants (CNVs) as susceptibility factors. We also sought to identify gene mechanisms common to groups of...

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Pescosolido MF, Gamsiz ED, Nagpal S, et al. Distribution of disease-associated copy number variants across distinct disorders of cognitive development. J Am Acad Child Adolesc Psychiatry. 2013;52(4):414-430.e14doi: 10.1016/j.jaac.2013.01.003.
Pescosolido, M. F., Gamsiz, E. D., Nagpal, S., & Morrow, E. M. (2013). Distribution of disease-associated copy number variants across distinct disorders of cognitive development. Journal of the American Academy of Child and Adolescent Psychiatry, 52(4), 414-430.e14. https://doi.org/10.1016/j.jaac.2013.01.003
Pescosolido, Matthew F, et al. "Distribution of disease-associated copy number variants across distinct disorders of cognitive development." Journal of the American Academy of Child and Adolescent Psychiatry vol. 52,4 (2013): 414-430.e14. doi: https://doi.org/10.1016/j.jaac.2013.01.003
Pescosolido MF, Gamsiz ED, Nagpal S, Morrow EM. Distribution of disease-associated copy number variants across distinct disorders of cognitive development. J Am Acad Child Adolesc Psychiatry. 2013 Apr;52(4):414-430.e14. doi: 10.1016/j.jaac.2013.01.003. PMID: 23582872; PMCID: PMC3774163.
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Familial mental retardation: a continuing dilemma.

Science (New York, N.Y.)

Zigler E.
PMID: 5333962
Science. 1967 Jan 20;155(3760):292-8. doi: 10.1126/science.155.3760.292.

The heterogeneous nature of mental retardation, as well as certain common practices of workers in the area, has resulted in a variety of conceptual am biguities. Considerable order could be brought to the area if, instead of viewing all...

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Zigler E. Familial mental retardation: a continuing dilemma. Science. 1967;155(3760):292-8doi: 10.1126/science.155.3760.292.
Zigler, E. (1967). Familial mental retardation: a continuing dilemma. Science (New York, N.Y.), 155(3760), 292-8. https://doi.org/10.1126/science.155.3760.292
Zigler, E. "Familial mental retardation: a continuing dilemma." Science (New York, N.Y.) vol. 155,3760 (1967): 292-8. doi: https://doi.org/10.1126/science.155.3760.292
Zigler E. Familial mental retardation: a continuing dilemma. Science. 1967 Jan 20;155(3760):292-8. doi: 10.1126/science.155.3760.292. PMID: 5333962.
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[Diagnostic investigations for an unexplained developmental disability].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Verloes A, Héron D, Billette de Villemeur T, Afenjar A, Baumann C, Bahi-Buisson N, Charles P, Faudet A, Jacquette A, Mignot C, Moutard ML, Passemard S, Rio M, Robel L, Rougeot C, Ville D, Burglen L, des Portes V.
PMID: 22245660
Arch Pediatr. 2012 Feb;19(2):194-207. doi: 10.1016/j.arcped.2011.11.014. Epub 2012 Jan 14.

Developmental disability/mental retardation is a major public health problem and a common cause of consultation in pediatrics, neuropediatrics, and genetics. Etiologies of mental retardation are highly heterogeneous. Diagnostic strategies have been explored in a small number of consensus publications,...

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Verloes A, Héron D, Billette de Villemeur T, et al. Stratégie d'exploration d'une déficience intellectuelle inexpliquée. [Diagnostic investigations for an unexplained developmental disability]. Arch Pediatr. 2012;19(2):194-207doi: 10.1016/j.arcped.2011.11.014.
Verloes, A., Héron, D., Billette de Villemeur, T., Afenjar, A., Baumann, C., Bahi-Buisson, N., Charles, P., Faudet, A., Jacquette, A., Mignot, C., Moutard, M. L., Passemard, S., Rio, M., Robel, L., Rougeot, C., Ville, D., Burglen, L., des Portes, V. (2012). Stratégie d'exploration d'une déficience intellectuelle inexpliquée. [Diagnostic investigations for an unexplained developmental disability]. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 19(2), 194-207. https://doi.org/10.1016/j.arcped.2011.11.014
Verloes, A, et al. "Stratégie d'exploration d'une déficience intellectuelle inexpliquée." [Diagnostic investigations for an unexplained developmental disability]. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 19,2 (2012): 194-207. doi: https://doi.org/10.1016/j.arcped.2011.11.014
Verloes A, Héron D, Billette de Villemeur T, Afenjar A, Baumann C, Bahi-Buisson N, Charles P, Faudet A, Jacquette A, Mignot C, Moutard ML, Passemard S, Rio M, Robel L, Rougeot C, Ville D, Burglen L, des Portes V. Stratégie d'exploration d'une déficience intellectuelle inexpliquée. [Diagnostic investigations for an unexplained developmental disability]. Arch Pediatr. 2012 Feb;19(2):194-207. doi: 10.1016/j.arcped.2011.11.014. Epub 2012 Jan 14. French. PMID: 22245660.
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Showing 1 to 12 of 61 entries