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Results 1 to 25 of 38492

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OMPHALOCELE, RADIAL RAY DEFECT AND DIAPHRAGMATIC HERNIA: ANOTHER CASE OF GERSHONI-BARUCH SYNDROME?OUDESLUIJS, G.Genetic counseling. 2014, Vol 25, Num 1, pp 77-79, issn 1015-8146, 3 p.Article

TERMINAL DELETION 6q SYNDROME WITH 11q PARTIAL TRISOMY MOSAICISM DUE TO MATERNAL BALANCED TRANSLOCATIONIMATAKA, G; OKUYA, M; HIRAO, J et al.Genetic counseling. 2014, Vol 25, Num 1, pp 63-67, issn 1015-8146, 5 p.Article

A RARE SUBTELOMERIC DELETION SYNDROME: WOLF HIRSCHHORN SYNDROMEZORLU, P; EKSIOGLU, A. S; OZKAN, M et al.Genetic counseling. 2014, Vol 25, Num 3, pp 299-303, issn 1015-8146, 5 p.Article

Development of motor planning for dexterity tasks in trisomy 21JOVER, Marianne; AYOUN, Catherine; BERTON, Catherine et al.Research in developmental disabilities (Print). 2014, Vol 35, Num 7, pp 1562-1570, issn 0891-4222, 9 p.Article

Examining the operant function of challenging behavior in young males with fragile X syndrome: A summary of 12 casesMACHALICEK, Wendy; McDUFFIE, Andrea; OAKES, Ashley et al.Research in developmental disabilities (Print). 2014, Vol 35, Num 7, pp 1694-1704, issn 0891-4222, 11 p.Article

Eye Movements Reveal Impaired Inhibitory Control in Adult Male Fragile X Premutation Carriers Asymptomatic for FXTASWONG, Ling M; GOODRICH-HUNSAKER, Naomi J; MCLENNAN, Yingratana et al.Neuropsychology. 2014, Vol 28, Num 4, pp 571-584, issn 0894-4105, 14 p.Article

GENETIC RISK SCORE FOR NONSYNDROMIC CLEFT LIP WITH OR WITHOUT CLEFT PALATE FOR A CHILEAN POPULATIONBLANCO, R; COLOMBO, A; SUAZO, J et al.Genetic counseling. 2014, Vol 25, Num 2, pp 143-149, issn 1015-8146, 7 p.Article

ISOLATED ECTRODACTYLY IN A NEWBORN WITH DOWN SYNDROMEKAVURT, S; CELIK, I. H; ADA, B. S et al.Genetic counseling. 2014, Vol 25, Num 2, pp 209-214, issn 1015-8146, 6 p.Article

Maternal well-being and child behavior in families with fragile X syndromeHAUSER, Claire T; KOVER, Sara T; ABBEDUTO, Leonard et al.Research in developmental disabilities (Print). 2014, Vol 35, Num 10, pp 2477-2486, issn 0891-4222, 10 p.Article

Nouns and predicates comprehension and production in children with Down syndromeBELLO, A; ONOFRIO, D; CASELLI, M. C et al.Research in developmental disabilities (Print). 2014, Vol 35, Num 4, pp 761-775, issn 0891-4222, 15 p.Article

PRENATAL DIAGNOSIS OF ISOCHROMOSOME 21p AND ISOCHROMOSOME 21q IN A FETUS WITH DOWN SYNDROMEYAKUT, S; SANHAL, C; MANGUOGLU, E et al.Genetic counseling. 2014, Vol 25, Num 3, pp 257-264, issn 1015-8146, 8 p.Article

PURE 9P TRISOMY DERIVED FROM A TERMINAL BALANCED UNRECIPROCAL TRANSLOCATIONBRAMBILA-TAPIA, A. J. L; NEIRA, V.A; VASQUEZ-VELASQUEZ, A. I et al.Genetic counseling. 2014, Vol 25, Num 3, pp 289-297, issn 1015-8146, 9 p.Article

Perceiving and acting in depth in Williams syndrome and typical developmentHUDSON, Kerry D; FARRAN, Emily K.Research in developmental disabilities (Print). 2014, Vol 35, Num 8, pp 1850-1855, issn 0891-4222, 6 p.Article

Predicting METs from the heart rate index in persons with Down syndromeAGIOVLASITIS, Stamatis; ROSSOW, Lindy M; VAN, Huimin et al.Research in developmental disabilities (Print). 2014, Vol 35, Num 10, pp 2423-2429, issn 0891-4222, 7 p.Article

Aging and sleep in Williams syndrome: Accelerated sleep deterioration and decelerated slow wave sleep decrementBODIZS, Róbert; GOMBOS, Ferenc; GERVAN, Patrícia et al.Research in developmental disabilities (Print). 2014, Vol 35, Num 12, pp 3226-3235, issn 0891-4222, 10 p.Article

Concrete and relational vocabulary: Comparison between Williams and Smith-Magenis syndromesGARAYZABAL HEINZE, Elena; OSORIO, Ana; LENS, María et al.Research in developmental disabilities (Print). 2014, Vol 35, Num 12, pp 3365-3371, issn 0891-4222, 7 p.Article

A NEW PATIENT WITH ANDERMANN SYNDROME: AN UNDERDIAGNOSED CLINICAL GENETICS ENTITY?DEGERLIYURT, A; AKGUMUS, G; CAGLAR, C et al.Genetic counseling. 2013, Vol 24, Num 3, pp 283-289, issn 1015-8146, 7 p.Article

AN EXTREMELY RARE CASE: OSTEOSCLEROTIC METAPHYSEAL DYSPLASIAKASAPKARA, C. S; KÜCÜKCONGAR, A; BOYUNAGA, O et al.Genetic counseling. 2013, Vol 24, Num 1, pp 69-74, issn 1015-8146, 6 p.Article

Contextual integration of causal coherence in people with Williams syndromeHSU, Ching-Fen.Research in developmental disabilities (Print). 2013, Vol 34, Num 10, pp 3332-3342, issn 0891-4222, 11 p.Article

Effects of whole body vibration training on body composition in adolescents with Down syndromeGONZALEZ-AGÜERO, Alejandro; MATUTE-LLORENTE, Angel; GOMEZ-CABELLO, Alba et al.Research in developmental disabilities (Print). 2013, Vol 34, Num 5, pp 1426-1433, issn 0891-4222, 8 p.Article

Infants with Down syndrome: Percentage and age for acquisition of gross motor skillsPEREIRA, Karina; PEDROLONGO BASSO, Renata; RODRIGUES LINDQUIST, Ana Raquel et al.Research in developmental disabilities (Print). 2013, Vol 34, Num 3, pp 894-901, issn 0891-4222, 8 p.Article

Long-term Impact of Parental Well-Being on Adult Outcomes and Dementia Status in Individuals With Down SyndromeESBENSEN, Anna J; MAILICK, Marsha R; SILVERMAN, Wayne et al.American journal on intellectual and developmental disabilities (Print). 2013, Vol 118, Num 4, issn 1944-7515, 294-309, 338 [17 p.]Article

PARTIAL TRISOMY 3p AND MONOSOMY 5p DIAGNOSED BY SPECTRAL KARYOTYPING (SKY)IMATAKA, G; TSUBOI, T; KURIBAYASHI, R et al.Genetic counseling. 2013, Vol 24, Num 4, pp 445-448, issn 1015-8146, 4 p.Article

TETRASOMY 12P PRESENTING WITH LONG APPENDIX: A PRENATAL CASEAYDIN, H; ARISOY, R; GECKINLI, B et al.Genetic counseling. 2013, Vol 24, Num 4, pp 439-440, issn 1015-8146, 2 p.Article

Wayfinding behaviour in Down syndrome: A study with virtual environmentsCOURBOIS, Yannick; FARRAN, Emily K; LEMAHIEU, Axelle et al.Research in developmental disabilities (Print). 2013, Vol 34, Num 5, pp 1825-1831, issn 0891-4222, 7 p.Article

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