Nanisme microcéphalique, arriération sévère, hypertonie, obésité et hypog&nitalisme chez deux frères : un nouveau syndrome? = Two brothers with severe mental and growth retardation, microcephaly, hypertonicity, obesity and hypogenitalism: a new syndromeDELOZIER-BLANCHET, C. D; HAENGGELI, C. A; ENGEL, E et al.Journal de génétique humaine. 1989, Vol 37, Num 4-5, pp 353-365, issn 0021-7743, 13 p.Article

A prospective study of the accuracy of ultrasound in predicting fetal microcephalyCHERVENAK, F. A; ROSENBERG, J; BRIGHTMAN, R. C et al.Obstetrics and gynecology (New York. 1953). 1987, Vol 69, Num 6, pp 908-910, issn 0029-7844Article

Atelencephalic microcephaly: craniofacial anatomy and morphologic comparisons with holoprosencephaly and anencephalySIEBERT, J. R; KOKICH, V. G; WARKANY, J et al.Teratology (Philadelphia, PA). 1987, Vol 36, Num 3, pp 279-285, issn 0040-3709Article

Disproportionate intra-uterine head growth and developmental outcomeBRENNAN, T. L; FUNK, S. G; FROTHINGHAM, T. E et al.Developmental medicine and child neurology (Print). 1985, Vol 27, Num 6, pp 746-750, issn 0012-1622Article

Nanisme microcéphalique primordial de type II : à propos d'un cas ayant terminé sa croissance = Type II primordial microcephalic dwarfism. Report of a patient with completed growthTHEAU, D; MAROTEAUX, P.Annales de pédiatrie (Paris). 1993, Vol 40, Num 5, pp 323-328, issn 0066-2097Article

Microcéphalie familiale héréditaire: étude clinique et génétique à propos de cinq cas = Familial hereditary microcephaly. Clinical and genetic findings in five casesNORES, J. M; VINOGRADOFF, M; BAROIS, A et al.La Semaine des hôpitaux de Paris. 1989, Vol 65, Num 26, pp 1619-1622, issn 0037-1777Article

Growth hormone treatment in children with sporadic primary microcephalySPADONI, G. L; CIANFARANI, S; BERNARDINI, S et al.American journal of diseases of children (1960). 1989, Vol 143, Num 11, pp 1282-1283, issn 0002-922X, 2 p.Article

Autosomal recessive nonsyndromal microcephaly with normal intelligenceTEEBI, A. S; AL-AWADI, S. A; WHITE, A. G et al.American journal of medical genetics. 1987, Vol 26, Num 2, pp 355-359, issn 0148-7299Article

Microcephaly: a review of genetic implications in its causationCOWIE, V. A.Journal of mental deficiency research. 1987, Vol 31, Num 3, pp 229-233, issn 0022-264XArticle

Neuropathology of Seckel syndrome in fetal stage with evidence of intrauterine developmental retardationHORI, A; TAMAGAWA, K; EBER, S. W et al.Acta neuropathologica. 1987, Vol 74, Num 4, pp 397-401, issn 0001-6322Article

Reduction of disruptive mealtime behavior by facial screening. A case study of a mentally retarded girl with long-term follow-upHORTON, S. V.Behavior modification. 1987, Vol 11, Num 1, pp 53-64, issn 0145-4455Article

GMS syndrome : a new dominant condition with goniodysgenesis, mental retardation, and short statureKUPCHIK, G. S; LUDMAN, M. D; RAAB, E. L et al.American journal of medical genetics. 1992, Vol 42, Num 1, pp 1-4, issn 0148-7299Article

Microencephaly: cortical hypoplasia induced by methylazoxymethanolSANBERG, P. R; MORAN, T. H; COYLE, J. T et al.Neurology and neurobiology. 1987, Vol 33, pp 253-278, issn 0736-4563Article

Neu laxova syndrome in two Egyptian familiesABDEL MEGUID, N; TEMTAMY, S. A.American journal of medical genetics. 1991, Vol 41, Num 1, pp 30-31, issn 0148-7299Article

Nager anomaly with severe facial involvement, microcephaly, and mental retardationPALOMEQUE, A; PASTOR, X; BALLESTA, F et al.American journal of medical genetics. 1990, Vol 36, Num 3, pp 356-357, issn 0148-7299, 2 p.Article

Syndrome familial associant : nanisme, microcéphalie, oligophrénie, épilepsie, surdité de dermatose. Un nouveau syndrome = Familial syndrome combining short stature, microcephaly, mental deficiency, seizures, hearing loss, and skin lesions: a new syndromeBOUDHINA, T; YEDES, A; KHIARI, S et al.Annales de pédiatrie (Paris). 1990, Vol 37, Num 6, pp 399-403, issn 0066-2097Article

Two brothers with facial anomalies, microcephaly, hypoplastic genitalia, and a failure of psychomotor developmentMACDERMOT, K. D; WINTER, R. M.American journal of medical genetics. 1989, Vol 32, Num 1, pp 60-62, issn 0148-7299, 3 p.Article

Case 27-2014: A 10-Month-Old Boy with Microcephaly and Episodic CyanosisSAHAI, Inderneel; MOCHIDA, Ganeshwaran H; GRABOWSKI, Eric F et al.The New England journal of medicine. 2014, Vol 371, Num 9, pp 847-858, issn 0028-4793, 12 p.Article

A Truncating Mutation of CEP135 Causes Primary Microcephaly and Disturbed Centrosomal FunctionHUSSAIN, Muhammad Sajid; BAIG, Shahid Mahmood; FROMMOLT, Peter et al.American journal of human genetics. 2012, Vol 90, Num 5, pp 871-878, issn 0002-9297, 8 p.Article

Chromosome 9p Deletion Syndrome and Sex Reversal: Novel Findings and Redefinition of the Critically Deleted RegionsONESIMO, Roberta; ORTESCHI, Daniela; SCALZONE, Maria et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 9, pp 2266-2271, issn 1552-4825, 6 p.Article

Head Circumference Growth Function as a Marker of Neurological Impairment in a Cohort of Microcephalic Infants and ChildrenCORONADO, Ricard; GIRALDO, Jesús; MACAYA, Alfons et al.Neuropediatrics. 2012, Vol 43, Num 5, pp 271-274, issn 0174-304X, 4 p.Article

Magnetic resonance imaging of the brain in adenylosuccinate lyase deficiency: a report of seven cases and a review of the literatureJURECKA, Agnieszka; JURKIEWICZ, Elzbieta; TYLKI-SZYMANSKA, Anna et al.European journal of pediatrics. 2012, Vol 171, Num 1, pp 131-138, issn 0340-6199, 8 p.Article

Microdeletion in Distal 17p13.1: A Recognizable Phenotype With Microcephaly, Distinctive Facial Features, and Intellectual DisabilityZEESMAN, Susan; KJAERGAARD, Susanne; HOVE, Hanne D et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 8, pp 1832-1836, issn 1552-4825, 5 p.Article

De Novo Duplication 11p13 Involving the PAX6 Gene in a Patient With Neonatal Seizures, Hypotonia, Microcephaly, Developmental Disability and Minor Ocular ManifestationsARADHYA, Swaroop; SMAOUI, Nizar; MARBLE, Michael et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 2, pp 442-444, issn 1552-4825, 3 p.Article

Ambiguous Genitalia, Microcephaly, Seizures, Bone Malformations, and Early Death: A Distinct MCA/MR SyndromeMEGARBANE, André; CHOUERY, Eliane; MIGNON-RAVIX, Cécile et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 5, pp 1147-1151, issn 1552-4825, 5 p.Article