Morphometric analysis and classification of the facial phenotype associated with fetal alcohol syndrome in 5‐ and 12‐year‐old children (English)
- New search for: Mutsvangwa, Tinashe E.M.
- New search for: Meintjes, Ernesta M.
- New search for: Viljoen, Dennis L.
- New search for: Douglas, Tania S.
- New search for: Mutsvangwa, Tinashe E.M.
- New search for: Meintjes, Ernesta M.
- New search for: Viljoen, Dennis L.
- New search for: Douglas, Tania S.
In:
American Journal of Medical Genetics Part A
;
152A
, 1
;
32-41
;
2010
- Article (Journal) / Electronic Resource
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Title:Morphometric analysis and classification of the facial phenotype associated with fetal alcohol syndrome in 5‐ and 12‐year‐old children
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Contributors:Mutsvangwa, Tinashe E.M. ( author ) / Meintjes, Ernesta M. ( author ) / Viljoen, Dennis L. ( author ) / Douglas, Tania S. ( author )
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Published in:American Journal of Medical Genetics Part A ; 152A, 1 ; 32-41
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Publisher:
- New search for: Wiley Subscription Services, Inc., A Wiley Company
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Publication date:2010-01-01
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Size:10 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Keywords:
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Source:
Table of contents – Volume 152A, Issue 1
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 1
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Word smithing in medical geneticsCohen, M. Michael Jr. et al. | 2010
- 4
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Proceedings from the 2009 genetic syndromes of the Ras/MAPK pathway: From bedside to bench and backRauen, Katherine A. / Schoyer, Lisa / McCormick, Frank / Lin, Angela E. / Allanson, Judith E. / Stevenson, David A. / Gripp, Karen W. / Neri, Giovanni / Carey, John C. / Legius, Eric et al. | 2010
- 25
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Systematized organoid epidermal nevus with eccrine differentiation, multiple facial and oral congenital scars, gingival synechiae, and blepharophimosis: A novel epidermal nevus syndromeCastori, Marco / Annessi, Giorgio / Castiglia, Daniele / Buffa, Vitaliano / Paradisi, Andrea / Cascone, Piero / Zambruno, Giovanna / Grammatico, Paola / Paradisi, Mauro et al. | 2010
- 32
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Morphometric analysis and classification of the facial phenotype associated with fetal alcohol syndrome in 5‐ and 12‐year‐old childrenMutsvangwa, Tinashe E.M. / Meintjes, Ernesta M. / Viljoen, Dennis L. / Douglas, Tania S. et al. | 2010
- 42
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Speech characteristics in neurofibromatosis type 1Alivuotila, Lotta / Hakokari, Jussi / Visnapuu, Vivian / Korpijaakko‐Huuhka, Anna‐Maija / Aaltonen, Olli / Happonen, Risto‐Pekka / Peltonen, Sirkku / Peltonen, Juha et al. | 2010
- 52
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The process of deciding about prophylactic surgery for breast and ovarian cancer: Patient questions, uncertainties, and communicationKlitzman, Robert / Chung, Wendy et al. | 2010
- 67
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Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian populationCampbell, Colleen A. / Della Santina, Charley C. / Meyer, Nicole C. / Smith, Nancy B. / Myrie, Oluwaseun A. / Stone, Edwin M. / Fukushima, Kuni / Califano, Joseph / Carey, John P. / Hansen, Marlan R. et al. | 2010
- 75
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Hypospadias in males with intrauterine growth restriction due to placental insufficiency: The placental role in the embryogenesis of male external genitaliaYinon, Yoav / Kingdom, John C.P. / Proctor, Leslie K. / Kelly, Edmond N. / Salle, Joao L. Pippi / Wherrett, Diane / Keating, Sarah / Nevo, Ori / Chitayat, David et al. | 2010
- 84
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Living with Costello syndrome: Quality of life issues in older individualsHopkins, Elizabeth / Lin, Angela E. / Krepkovich, Katherine E. / Axelrad, Marni E. / Sol‐Church, Katia / Stabley, Deborah L. / Hossain, Jobayer / Gripp, Karen W. et al. | 2010
- 91
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Analysis of short‐term behavioral effects of dietary cholesterol supplementation in Smith–Lemli–Opitz syndromeTierney, Elaine / Conley, Sandra K. / Goodwin, Halima / Porter, Forbes D. et al. | 2010
- 96
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Diagnostic utility of daytime salivary melatonin levels in Smith–Magenis syndromeChik, Constance L. / Rollag, Mark D. / Duncan, Wallace C. / Smith, Ann C.M. et al. | 2010
- 102
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Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagiaD'Angelo, Carla S. / Kohl, Ilana / Varela, Monica Castro / de Castro, Cláudia I.E. / Kim, Chong A. / Bertola, Débora R. / Lourenço, Charles M. / Koiffmann, Célia P. et al. | 2010
- 111
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Ectodermal dysplasia‐like syndrome with mental retardation due to contiguous gene deletion: Further clinical and molecular delineation of del(2q32) syndromeRifai, Laila / Port‐Lis, Marylin / Tabet, Anne‐Claude / Bailleul‐Forestier, Isabelle / Benzacken, Brigitte / Drunat, Séverine / Kuzbari, Suzanne / Passemard, Sandrine / Verloes, Alain / Aboura, Azzedine et al. | 2010
- 118
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An unusual severe vascular case of pseudoxanthoma elasticum presenting as generalized arterial calcification of infancyLe Boulanger, G. / Labrèze, C. / Croué, A. / Schurgers, L.J. / Chassaing, N. / Wittkampf, T. / Rutsch, F. / Martin, L. et al. | 2010
- 124
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Loss of N‐acetylglucosamine‐1‐phosphotransferase gamma subunit due to intronic mutation in GNPTG causes mucolipidosis type III gamma: Implications for molecular and cellular diagnosticsPohl, Sandra / Encarnacão, Marisa / Castrichini, Monica / Müller‐Loennies, Sven / Muschol, Nicole / Braulke, Thomas et al. | 2010
- 133
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Various types of LRP5 mutations in four patients with osteoporosis‐pseudoglioma syndrome: Identification of a 7.2‐kb microdeletion using oligonucleotide tiling microarrayNarumi, Satoshi / Numakura, Chikahiko / Shiihara, Takashi / Seiwa, Chizuru / Nozaki, Yasuyuki / Yamagata, Takanori / Momoi, Mariko Y. / Watanabe, Yoriko / Yoshino, Makoto / Matsuishi, Toyojiro et al. | 2010
- 141
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A novel UBE3A truncating mutation in large Tunisian Angelman syndrome pedigreeAbaied, L. / Trabelsi, M. / Chaabouni, M. / Kharrat, M. / Kraoua, L. / M'rad, R. / Tebib, N. / Maazoul, F. / Chaabouni, H. et al. | 2010
- 147
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Genetic counseling for schizophrenia: A review of referrals to a provincial medical genetics program from 1968 to 2007Hunter, M.J. / Hippman, Catriona / Honer, William G. / Austin, Jehannine C. et al. | 2010
- 153
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Fowler syndrome—A clinical, radiological, and pathological study of 14 casesWilliams, Denise / Patel, Chirag / Fallet‐Bianco, Catherine / Kalyanasundaram, Karthik / Yacoubi, Mohamed / Déchelotte, Pierre / Scott, Rosemary / Bazin, Anne / Bessières, Bettina / Marton, Tamas et al. | 2010
- 161
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Floating‐Harbor syndrome associated with middle ear abnormalitiesHendrickx, Jan‐Jaap / Keymolen, Kathelijn / Desprechins, Brigitte / Casselman, Jan / Gordts, Frans et al. | 2010
- 165
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Novel cardiac findings in periventricular nodular heterotopiaJefferies, John L. / Taylor, Michael D. / Rossano, Joseph / Belmont, John W. / Craigen, William J. et al. | 2010
- 169
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Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C‐terminal region of RUNX2El‐Gharbawy, Areeg H. / Peeden, Joseph N. Jr. / Lachman, Ralph S. / Graham, John M. Jr. / Moore, Stephen R. / Rimoin, David L. et al. | 2010
- 175
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Deletion of the CUL4B gene in a boy with mental retardation, minor facial anomalies, short stature, hypogonadism, and ataxiaIsidor, Bertrand / Pichon, Olivier / Baron, Sabine / David, Albert / Le Caignec, Cédric et al. | 2010
- 181
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Two patients with EP300 mutations and facial dysmorphism different from the classic Rubinstein–Taybi syndromeBartsch, Oliver / Labonté, Janette / Albrecht, Beate / Wieczorek, Dagmar / Lechno, Stanislav / Zechner, Ulrich / Haaf, Thomas et al. | 2010
- 185
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A paternally transmitted complex chromosomal rearrangement (CCR) involving chromosomes 2, 6, and 18 includes eight breakpoints and five insertional translocations (ITs) through three generationsGruchy, Nicolas / Barreau, Morgane / Kessler, Ketty / Gourdier, Dominique / Leporrier, Nathalie et al. | 2010
- 191
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Left ventricular noncompaction: A rare disorder in adults and its association with 1p36 chromosomal anomalyDod, Harvinder S. / Bhardwaj, Ravindra / Hummel, Marybeth / Morise, Anthony P. / Batish, Satdev / Warden, Bradford E. / Beto, Robert J. / Jain, Abnash C. et al. | 2010
- 196
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A de novo 8.8‐Mb deletion of 21q21.1–q21.3 in an autistic male with a complex rearrangement involving chromosomes 6, 10, and 21Haldeman‐Englert, Chad R. / Chapman, Kimberly A. / Kruger, Hillary / Geiger, Elizabeth A. / McDonald‐McGinn, Donna M. / Rappaport, Eric / Zackai, Elaine H. / Spinner, Nancy B. / Shaikh, Tamim H. et al. | 2010
- 203
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Wolf–Hirschhorn syndrome and ectrodactyly: New findings and a review of the literatureShanske, Alan L. / Yachelevich, Naomi / Ala‐Kokko, Leena / Leonard, Jay / Levy, Brynn et al. | 2010
- 209
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Chromosome 6 between‐arm intrachromosomal insertion with intrasegmental double inversion: A four‐break modelWang, Jia‐Chi / Dang, Linda / Fisker, Thomas et al. | 2010
- 212
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Risk of breast cancer not increased in translocation 11;22 carriers: Analysis of 80 pedigreesCarter, Melissa T. / Barrowman, Nicholas J. / St.Pierre, Stephanie A. / Emanuel, Beverly S. / Boycott, Kym M. et al. | 2010
- 215
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CHN1 mutations are not a common cause of sporadic Duane's retraction syndromeMiyake, Noriko / Andrews, Caroline / Fan, Wen / He, Wei / Chan, Wai‐Man / Engle, Elizabeth C. et al. | 2010
- 218
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An unusual phenotypic presentation of trisomy 18Patel, Sonal / Yazdani, Malektaj / Barkemeyer, Brian / Lacassie, Yves et al. | 2010
- 222
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Further evidence for EpCAM as the gene for congenital tufting enteropathySivagnanam, Mamata / Schaible, Tiffany / Szigeti, Reka / Byrd, Robert H. / Finegold, Milton J. / Ranganathan, Sarangarajan / Gopalakrishna, G.S. / Tatevian, Nina / Kellermayer, Richard et al. | 2010
- 225
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GAPO syndrome associated with craniofacial vascular malformationCastrillon‐Oberndorfer, Gregor / Seeberger, Robin / Bacon, Claire / Engel, Michael / Ebinger, Friedrich / Thiele, Oliver Christian et al. | 2010
- 228
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Variegated aneuploidy and ring chromosome syndromes overlapRivera, Horacio / Domínguez, María G. et al. | 2010
- 230
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An 18‐year follow‐up report on an infant with a duplication of 9q34Youngs, Erin L. / McCord, Timothy / Hellings, Jessica A. / Spinner, Nancy B. / Schneider, Adele / Butler, Merlin G. et al. | 2010
- 234
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Ring chromosome 14 mosaicism: An unusual case associated with developmental delay and epilepsy, characterized by genome array‐CGHNucaro, Anna Lisa / Falchi, Melania / Pisano, Tiziana / Rossino, Rossano / Boscarelli, Francesca / Stoico, Giusi / Milia, Angela / Montaldo, Caterina / Cianchetti, Carlo / Pruna, Dario et al. | 2010
- 237
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Phenotypic map in ring 14 syndromeZollino, Marcella / Orteschi, Daniela / Neri, Giovanni et al. | 2010
- 238
-
Hedgehog signaling: Endocrine gland development and functionCohen, M. Michael Jr. et al. | 2010
- 245
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Review of the recently defined molecular mechanisms underlying thanatophoric dysplasia and their potential therapeutic implications for achondroplasiaMartínez‐Frías, María Luisa / de Frutos, Cristina A. / Bermejo, Eva / Nieto, M. Angela / ECEMC Working Group et al. | 2010
- 256
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Book reviewSharpe, Neil F. et al. | 2010
- 258
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Mild Wolf–Hirschhorn phenotype in a girl with unbalanced t(4p;12p) translocation without seizuresGalasso, Cinzia / Lo‐Castro, Adriana / El‐Malhany, Nadia / Zollino, Marcella / Murdolo, Marina / Orteschi, Daniela / Manca Bitti, Maria Luisa / Curatolo, Paolo et al. | 2010
- 262
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Homozygosity for the common mutation c.1085dupT in the ZMPSTE24 gene in a Mennonite baby with restrictive dermopathy and placenta abruptionLi, Chumei et al. | 2010
- 264
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Holoprosencephaly‐diencephalic hamartoma: Sequence or pleiotropy?Castori, Marco et al. | 2010
- C1
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American Journal of Medical Genetics Part A: Volume 152A, Number 1, January 2010| 2010
- fm i
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Table of Contents, Volume 152A, Number 1, January 2010| 2010
- fm ix
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In this issueLevenson, Deborah et al. | 2010
- fm ix
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College athletes should get sickle cell trait tests, NCAA advisesLevenson, Deborah et al. | 2010
- fm ix
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More African American genetic counselors neededLevenson, Deborah et al. | 2010
- fm vii
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Draft recommendations suggest HHS exempt gene patents from infringement liabilityLevenson, Deborah et al. | 2010
- fm viii
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ACLU case against Myriad GeneticsLevenson, Deborah et al. | 2010