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  American Journal of Medical Genetics Part A: Volume 140A, Issue 13

  Pages: 1357-1490

  1 July 2006

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Introduction

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Split hand foot malformation (SHFM): An introduction^†

Alan L. Shanske, 

• Pages: 1357-1358
• First Published: 10 May 2006

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Research Reviews

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The expanding panorama of split hand foot malformation^†

Donald Basel,  Michael W. Kilpatrick,  Petros Tsipouras, 

• Pages: 1359-1365
• First Published: 08 June 2006

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Dlx homeobox gene control of mammalian limb and craniofacial development^†

Petra Kraus,  Thomas Lufkin, 

• Pages: 1366-1374
• First Published: 10 May 2006

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Research Articles

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Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation^†

David B. Everman,  Chad T. Morgan,  Robert Lyle,  Mary E. Laughridge,  Michael J. Bamshad,  Katie B. Clarkson,  Randall Colby,  Fiorella Gurrieri,  A. Micheil Innes,  Jacquelyn Roberson,  Connie Schrander-Stumpel,  Hans van Bokhoven,  Stylianos E. Antonarakis,  Charles E. Schwartz, 

• Pages: 1375-1383
• First Published: 07 June 2006

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Split-hand/split-foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the region^†

Robert Lyle,  Uppala Radhakrishna,  Jean-Louis Blouin,  Sarantis Gagos,  David B. Everman,  Corinne Gehrig,  Celia Delozier-Blanchet,  Jitendra V. Solanki,  Uday C. Patel,  Swapan K. Nath,  Fiorella Gurrieri,  Giovanni Neri,  Charles E. Schwartz,  Stylianos E. Antonarakis, 

• Pages: 1384-1395
• First Published: 11 May 2006

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Pattern of p63 mutations and their phenotypes—update^†

Tuula Rinne,  Ben Hamel,  Hans van Bokhoven,  Han G. Brunner, 

• Pages: 1396-1406
• First Published: 11 May 2006

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Research Reviews

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T-genes and limb bud development^†

Mary King,  Jelena S. Arnold,  Alan Shanske,  Bernice E. Morrow, 

• Pages: 1407-1413
• First Published: 10 May 2006

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Research Articles

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Using the TBX5 transcription factor to grow and sculpt the heart^†

Cathy J. Hatcher,  Deborah A. McDermott, 

• Pages: 1414-1418
• First Published: 11 May 2006

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Genotype–phenotype correlations in mapped split hand foot malformation (SHFM) patients^†

Alison M. Elliott,  Jane A. Evans, 

• Pages: 1419-1427
• First Published: 10 May 2006

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Clinical and epidemiological findings in patients with central ray deficiency: Split hand foot malformation (SHFM) in Manitoba, Canada^†

Alison M. Elliott,  Martin H. Reed,  Albert E. Chudley,  Bernard N. Chodirker,  Jane A. Evans, 

• Pages: 1428-1439
• First Published: 03 May 2006

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Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: Clinical and genetic analysis^†

Mohammed Naveed,  Mahmoud T. Al-Ali,  Sabita K. Murthy,  Sarah Al-Hajali,  Najib Al-Khaja,  Samuel Deutsch,  Armand Bottani,  Stylianos E. Antonarakis,  Swapan K. Nath,  Uppala Radhakrishna, 

• Pages: 1440-1446
• First Published: 10 May 2006

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Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndrome^†

Casey M. Rand,  Debra E. Weese-Mayer,  Brion S. Maher,  Lili Zhou,  Mary L. Marazita,  Elizabeth M. Berry-Kravis, 

• Pages: 1447-1452
• First Published: 08 June 2006

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Research Letters

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3′ UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: Haplotype analysis^†

Brion S. Maher,  Mary L. Marazita,  Casey Rand,  Lili Zhou,  Elizabeth M. Berry-Kravis,  Debra E. Weese-Mayer, 

• Pages: 1453-1457
• First Published: 11 May 2006

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Clinical Reports

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Autosomal dominant atretic cephalocele with phenotype variability: Report of a Brazilian family with six affected in four generations^†

D.R. Carvalho,  L.R. Giuliani,  G.N. Simão,  A.C. Santos,  J.M. Pina-Neto, 

• Pages: 1458-1462
• First Published: 22 May 2006

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Mosaicism for a full mutation, premutation, and deletion of the CGG repeats results in 22% FMRP and elevated FMR1 mRNA levels in a high-functioning fragile X male^†

Xiao-Dong Han,  Berkley R. Powell,  Judith L. Phalin,  Farid F. Chehab, 

• Pages: 1463-1471
• First Published: 07 June 2006

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Research Letters

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A germline PTEN mutation with manifestations of prenatal onset and verrucous epidermal nevus^†

Mustafa Tekin,  Burcu Öztürk Hişmi,  Suat Fitoz,  Fatoş Yalçınkaya,  Mesiha Ekim,  Aydan Kansu,  Mehmet Ertem,  Gülhis Deda,  Ercan Tutar,  Saadet Arsan,  Xiao-Ping Zhou,  Robert Pilarski,  Charis Eng,  Nejat Akar, 

• Pages: 1472-1475
• First Published: 02 June 2006

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Thanatophoric dysplasia type 2 with encephalocele during the second trimester^†

Dongzhi Li,  Can Liao,  Xiaoyan Ma,  Qiuming Li,  Xuewei Tang, 

• Pages: 1476-1477
• First Published: 02 June 2006

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Additional mitochondrial DNA mutations may explain extra-ocular involvement in LHON^†

L. Spruijt,  J.E. Hoogendijk,  A.T.M. Hendrickx,  I.F. de Coo,  P.A. Doevendans,  P.T.V.M. de Jong,  W.G.M. Spliet,  H. Kroes,  H.J. Smeets, 

• Pages: 1478-1481
• First Published: 12 June 2006

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Book Reviews

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Book review^†

Robert K. Koenekoop, 

• Page: 1482
• First Published: 11 May 2006

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Correspondence

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Problems in the naming of genes^†

M. Michael Cohen Jr, 

• Pages: 1483-1484
• First Published: 22 May 2006

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The use of inappropriate, demeaning, and pejorative terminology in gene nomenclature: A comment on Feingold^†

Mark D. Ludman, 

• Pages: 1485-1486
• First Published: 11 May 2006

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Keutel syndrome with overlapping features of cutis laxa: A new variant^†

Arti Nanda,  Jehoram T. Anim,  Meshal Al-Gareeb,  Qasem A. Alsaleh, 

• Pages: 1487-1489
• First Published: 26 April 2006

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Response to letter by Arti Nanda et al.^†

Bernard A. Cohen,  Simeon A. Boyadjiev, 

• Page: 1490
• First Published: 07 June 2006

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