The Molecular Genetics of HoloprosencephalyROESSLER, Erich; MUENKE, Maximilian.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 1, pp 52-61, issn 1552-4868, 10 p.Article

Abnormal Sterol Metabolism in HoloprosencephalyHAAS, Dorothea; MUENKE, Maximilian.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 1, pp 102-108, issn 1552-4868, 7 p.Article

Multiple hits during early embryonic development: Digenic diseases and holoprosencephalyMING, Jeffrey E; MUENKE, Maximilian.American journal of human genetics. 2002, Vol 71, Num 5, pp 1017-1032, issn 0002-9297, 16 p.Article

From the Black Widow Spider to Human Behavior: Latrophilins, a Relatively Unknown Class of G Protein-Coupled Receptors, Are Implicated in Psychiatric DisordersMARTINEZ, Ariel F; MUENKE, Maximilian; ARCOS-BURGOS, Mauricio et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2011, Vol 156, Num 1, pp 1-10, issn 1552-4841, 10 p.Article

HoloprosencephalyMUENKE, Maximilian; SOLOMON, Benjamin; ODENT, Sylvie et al.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 1, issn 1552-4868, 204 p.Serial Issue

Review : Genetics of Attention Deficit/Hyperactivity DisorderWALLIS, Deeann; RUSSELL, Heather F; MUENKE, Maximilian et al.Journal of pediatric psychology. 2008, Vol 33, Num 10, pp 1085-1099, issn 0146-8693, 15 p.Article

Non-syndromic hemihyperplasia in a male and his motherSLAVOTINEK, Anne M; COLLINS, Michael T; MUENKE, Maximilian et al.American journal of medical genetics. 2003, Vol 121A, Num 1, pp 47-51, issn 0148-7299, 5 p.Article

Current Recommendations for the Molecular Evaluation of Newly Diagnosed Holoprosencephaly PatientsPINEDA-ALVAREZ, Daniel E; DUBOURG, Christèle; DAVID, Véronique et al.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 1, pp 93-101, issn 1552-4868, 9 p.Article

Cyclopia (Synophthalmia) in Smith-Lemli-Opitz Syndrome: First Reported Case and Consideration of MechanismWEAVER, David D; SOLOMON, Benjamin D; AKIN-SAMSON, Kelly et al.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 1, pp 142-145, issn 1552-4868, 4 p.Article

Holoprosencephaly: A Mythologic and Teratologic DistillateCOHEN, M. Michael.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 1, pp 8-12, issn 1552-4868, 5 p.Article

Neuropathology of HoloprosencephalyMARCORELLES, Pascale; LAQUERRIERE, Annie.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 1, pp 109-119, issn 1552-4868, 11 p.Article

Early Pathogenesis of HoloprosencephalySHIOTA, Kohei; YAMADA, Shigehito.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 1, pp 22-28, issn 1552-4868, 7 p.Article

Epilepsy in Muenke Syndrome: FGFR3-Related CraniosynostosisAGOCHUKWU, Nneamaka B; SOLOMON, Benjamin D; GROPMAN, Andrea L et al.Pediatric neurology. 2012, Vol 47, Num 5, pp 355-361, issn 0887-8994, 7 p.Article

Holoprosencephaly and Holoprosencephaly-Like Phenotypes: Review of Facial and Molecular Findings in Patients From a Craniofacial Hospital in BrazilRICHIERI-COSTA, Antonio; ARILHO RIBEIRO, Lucilene.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 1, pp 149-157, issn 1552-4868, 9 p.Article

Neuroimaging Advances in Holoprosencephaly: Refining the Spectrum of the Midline MalformationHAHN, Jin S; BARNES, Patrick D.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 1, pp 120-132, issn 1552-4868, 13 p.Article

Holoprosencephaly and Ectrodactyly: Report of Three New Patients and Review of the LiteratureKEATON, Amelia A; SOLOMON, Benjamin D; VAN ESSEN, Anthonie J et al.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 1, pp 170-175, issn 1552-4868, 6 p.Article

Epidemiology of Holoprosencephaly: Prevalence and Risk FactorsORIOLI, Iêda M; CASTILLA, Eduardo E.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 1, pp 13-21, issn 1552-4868, 9 p.Article

Holoprosencephaly-Polydactyly syndrome : In search of an etiologyCORDERO, Dwight R; BENDAVID, Claude; SHANSKE, Alan L et al.European journal of medical genetics. 2008, Vol 51, Num 2, pp 106-112, issn 1769-7212, 7 p.Article

The decision to continue: The experiences and needs of parents who receive a prenatal diagnosis of holoprosencephalyREDLINGER-GROSSE, Krista; BERNHARDT, Barbara A; BERG, Kate et al.American journal of medical genetics. 2002, Vol 112, Num 4, pp 369-378, issn 0148-7299, 10 p.Article

CFC1 mutations in patients with transposition of the great arteries and double-outlet right ventricleGOLDMUNTZ, Elizabeth; BAMFORD, Richard; KARKERA, Jayaprakash D et al.American journal of human genetics. 2002, Vol 70, Num 3, pp 776-780, issn 0002-9297Article

Mutational analysis of the Sonic Hedgehog gene in 220 newborns with oral clefts in a south American (ECLAMC) ponulationORIOLI, Iêda M; VIEIRA, Alexandre R; CASTILLA, Eduardo E et al.American journal of medical genetics. 2002, Vol 108, Num 1, pp 12-15, issn 0148-7299Article

SONIC HEDGEHOG mutations causing human holoprosencephaly impair neural patterning activitySCHELL-APACIK, Can; RIVERO, Mariel; KNEPPER, Jessica L et al.Human genetics. 2003, Vol 113, Num 2, pp 170-177, issn 0340-6717, 8 p.Article

Holoprosencephaly Flashcards: A Summary for the ClinicianSOLOMON, Benjamin D; PINEDA-ALVAREZ, Daniel E; MERCIER, Sandra et al.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 1, pp 3-7, issn 1552-4868, 5 p.Article

Holoprosencephaly and Agnathia Spectrum: Presentation of Two New Patients and Review of the LiteratureKAUVAR, Emily F; SOLOMON, Benjamin D; CURRY, Cynthia J. R et al.American journal of medical genetics. Part C, Seminars in medical genetics. 2010, Vol 154, Num 1, pp 158-169, issn 1552-4868, 12 p.Article

Screening of Human LPHN3 for Variants With a Potential Impact on ADHD SusceptibilityDOMENE, Sabina; STANESCU, Horia; WALLIS, Deeann et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2011, Vol 156, Num 1, pp 11-18, issn 1552-4841, 8 p.Article