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133 TABLE 27, ANTERIOR NEUROPORE CLOSURE BY STAGES S tages Expe r I men ta I s (?) Open C I osed controts(%) Open e I osed 7 I 12(4.26) 15ß.32) 0 (0) 0 (0) ¡2(8.16) o(o) 16(1o.BB) o(o) 9 24 (8.5 r) 0 (0) 21(1t+.2-9) 0 (0) 10 tl 12 13 l3 (4. 61 ) 6(2.13) 2(o .71, 2(0.71) r I (3.90) 23 (8. 16) 10 (3. 55) 21(7 .45) 2(1.36') l1(7.48) 2(1.36) 12(8.16) 1(0.68) 8(5.44) o(o) r3(8.84) r4 15 16 1 (0.35) 2(0.71) 0 (0) 40(r4.18) 23ß.16') 20(7.09) o(o) 2(1.36) 0(0) 7$.76) o(o) r3(8.84) 17 18 19 1 (0. 35) r (0. 35) o (o) 23 (8. 16) 21(7.45) 8 (2. 84) I (0.68) 8(5.44) 0(0) 5(3.40) 0(0) 10(6.80) 20 0 (0) 3(r.06) 0 (0) 3 (2.04) Totals Numbers of Embryos
Fig. 31 . Percentêges of experinental and control embryos with an open or cìosed anterior neuropore at each Stage. Open anterior neuropore after Stage 12 regarded as an open braìn defect,
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E}4BRYOGENES IS OF EXPERIHENTALLY I
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MY PARENTS c.J.H. G. M.
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lt Congenital malformêtlons of the
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TABLE OF CONTENTS SECT ION PAGE 1 I
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},I.ATE R I ALS 3.1 THE CHICK EI4BR
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vt I I 6.3.2 Stage 10 Experímentel
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9 APPENDTCES 378 APPENDIX A . 379 1
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1.1 TERATOLOGY Birth defects have a
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4 of the complexity of normal devel
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6 flat, exposed plaque of neural ti
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8 However, several early embryos in
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.1- 5
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l2 2.1 ErI0L0rL!! fïE qYs34t!1!!jr
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4 which has rema¡ned fairly consta
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6 and about 112 after two (Laure,nc
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l8 ln some very early human embryos
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2l and kinky-ta¡l as disorders of
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23 Vogel and McClenahan (1952) tnus
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I'IATE R IALS 25
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27 lf necessary, eggs were stored a
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FÍg. 5. lncubator allowing precise
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3l 4. r sELEcr I oN !F EGGq 4.1,1 .
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uler. Accurate Staging (Hamburger a
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.\lz '?. t
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Fis. I AsB, Windowìng followed by
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Fis. 9 Aã8. t/indow?ng followed by
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42 ( \--l /) ^ ) t0
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44 serîal sectlonlng a camera luci
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46 Thus the embryos selected for se
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48 TABLE 3. srAGE t0 El,tBRyos (cno
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50 TABLE 5 , Reg i ons srAGE 13:16'
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52 4.8.4 HistologÌcal_De:plþtÍon
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5 RESULTS OF TERAÎOLOGICAL PROCEDU
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(c) deaths and defects in the survi
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Fi g. Percentagcs of early deaths a
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6o MoRTALtTY, AFTER ì,'tNpowtNq,AT
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TABLE B.'DEVEIOPI{ENT'AFTER'WINDOIi
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TABLE 9. ¡4ALFORMATIONS PRODUCED'B
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N=231 ffil e ooyi ffi s oays [il t2
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6B TABLEt loj lloRTALtTy AFTER VtBR
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70 5,3.2 Pa-rôf i Idì ¿irid PIè
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TABLE 13; MALFORI4ATIONS AFTER PLAS
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41 13 0 23 No l^l i ndow Control s
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Fíg. Percentages of early deaths a
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78 ALBUMEN INTRODUCTION Analysís o
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0 1 0 0 a o TABLE 17. I'lALF0RÌ1AT
Page 97 and 98: N Eorly Deothi N=10ó N a ú, o d,
Page 99 and 100: 103 51 52 28 14 4 6 No W î ndow Co
Page 101 and 102: Fi g. 14. Percentages of early deat
Page 103 and 104: 88 AtR qELL, REEXPANSI0N Analysls o
Page 105 and 106: 90 5.4 BACTERt4L CUTTURE 0F UlNpohr
Page 107 and 108: 92 TABLE 22. ¡¡UI'ISELTS OF PLATE
Page 109 and 110: 94 6.1 EMBRY0ûIIES I s 0L 0!!\- NE
Page 111 and 112: Fis. I5 A¿8, Range of s izes (mm.)
Page 113 and 114: Figs. 16 AaB.. Range of sizes (mm.
Page 115 and 116: 100 6.1.2 f4ortal í!y with Vsrying
Page 117 and 118: 421.. 26 25 I (3.85) 20 (76 .92) 1
Page 119 and 120: 00 N Eorly Deoths ,n -¡ F- ô- xu.
Page 121 and 122: ì06 Degrees of Freedom 12 Chi Squa
Page 123 and 124: hzE 53 42C z5 51(96.4)2\(96) 2(3.77
Page 125 and 126: ffil Op"n Anterior Neuropore I I0 N
Page 127 and 128: N=380 El Ovol Rhonnboid 'Sinus ì l
Page 129 and 130: Øl Open Broin Defecls N=384 ffi F"
Page 131 and 132: ligr. 21 - 30. Camera lucida drawin
Page 133 and 134: Fi s. 22. lrregular open anteríor
Page 135 and 136: lmm OPEN BRAIN DEFECT Á,NOPHTHALMI
Page 137 and 138: lmm OVAL RHOMBOID S¡NUS 48 HOURS S
Page 139 and 140: FiS. 26, Open neural folds extendin
Page 141 and 142: t-l lmm IATER OPEN CORD DEFECT . RE
Page 143 and 144: l2B t--l lmm EARLY OPEN CORD DEFECT
Page 145 and 146: Fis. 30. Large caudal cyst Ìn an o
Page 147: 132 6.1 .4 DeveloÞñent of oÞen N
Page 151 and 152: 36 TABLE ?8. RH0I4B0lD stNUs ctôs
Page 153 and 154: N=38o H ovol Rhomboid sinus l^ r38
Page 155 and 156: F¡ S. 33. Percentages Õf open cor
Page 157 and 158: 142 6.1.5 Distríbution of 0pen Cor
Page 159 and 160: Fi s. "l! Percentage distrìbution
Page 161 and 162: lrregul ar (Z) somi te be low level
Page 163 and 164: ì48 N=2ó4 ffi m Regulor Cord Defe
Page 165 and 166: Fis. 36. Percentage distrîbution o
Page 167 and 168: 152 6.2 sPtIA! LFVELS 0F oPEN CORp
Page 169 and 170: Fìgs. 37'38, Vertebral defecrs in
Page 171 and 172: CERVICAT THORACIC LUMBAR FUSED CAUD
Page 173 and 174: ---l r r'I * 40
Page 175 and 176: t59 a) spîna bif¡da occulta is se
Page 177 and 178: :al . '**Ç- 4 ff, À(,) ftø 9-' o
Page 179 and 180: 162 lmnediately after closure, sepa
Page 181 and 182: 164 Hensenrs node and the primitive
Page 183 and 184: -l :: l 48 I 49 i :. t: .lì 50 ì:
Page 185 and 186: t67 somite area (through asymmetry
Page 187 and 188: t69 ln both embryos the volume of n
Page 189 and 190: 171 The rhomblc roof became membran
Page 191 and 192: 173 At areas of myeloschisîs conta
Page 193 and 194: 175 neurêl tîssue wíth mesoderm
Page 195 and 196: t77 e) encroachment of somitîc mes
Page 197 and 198: ôt rf) , ,,. ì _ ^iiir¡:ù\. I r
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l 55 56 57 58 59 ó0
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Fiss. 65 Early myeloschisis in a St
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fiSr. 71 - 76. Later myeloschisis i
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Fiss. 77 -82. Early myelodysplesia
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FÌgs. B3 - BB. Later myelodysplas
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Figs, 89 - 91. Processíng artifact
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ì86 6.3.10 SequenJ¡¿il ll lúSti
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Fígs. 95 - 102, Sequentiêl drawin
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l9o EVERsToN: srAGE rf (o r o+) o @
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@ @@ "@ @ e q q a a 192 CoNTROL: ST
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MYELOSCHTSTS: STAGE tZ (tZeïl OOG
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coNTRO[: STAGE tó (ro c zz) . a@ Q
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G (õ--==: \z-- HEMTMYELIA: STAGE t
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Som i te Defects contact none sePa
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Somite Som i te Contact Defects N'
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Som i te Contact Som i te Defects c
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none none N) o o\ B r8c 23 12 good
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separat ion none contact/ none sepa
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Regíon Embryo Stage Conditîon Neu
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none none none none none none l'.J
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18E 10 13- vëry poor closed 0 cove
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separãtion none contact none conta
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Regíon Embryo Stage Condition Neur
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separation none sepâ ra t îon non
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separâtion none sepa ra t ion sepa
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Reglon Embryo Stagd cond¡t¡on Neu
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none none none none N) NJ .{ A A A
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contact/ none separatlon contact no
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Region Embryo Stage Conditlon Neura
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TABLE 38D. STAOE 17.20 CONTROL AND
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Reglon Embryo Stage Condition Neura
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428 72 20 closed covered none conta
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239 neural tissue ât the later sta
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241 The control group (Table 99 ) s
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TABLE 39. APPEARANCE OF I,'HOLE EI4
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TABLE 40. APPEARANCE OF }/HOLE EI"I
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closed closed c I osed c I osed c I
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249 6.6 pEVEL0PMENT 0F rH!_¡Ho|4gl
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Emb ryo Stage Rhombîc Roóf Neural
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CDE D'E DE CDE DE DE DE D BCD BC BC
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TABLE q6,. STAGE 17-20 CoNTRoI AND
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Figs- 10J - i11. Development of the
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Fî s. tub. Thick rhombic roof in 5
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Fig. 109 Hernbranous rhombic roof w
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260 6.7 HrqroLoctcAL, cHANgË Assoc
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TABLE 47. CONTROL EMBRYoS.HISTOLOGI
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0 0 0 0 0 0 0 0 0 0 o 0 0 0 0 0 0 N
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42c 21 zo B c D E 0000 00 00 00 1\.
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l\t q\ 1oE 26 16 30E 59 16 3oE 77 1
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0 0 0 0 0 0 0 0 0 0 0 0 N) .{ Embry
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l\) \l N D E 00 00 0 0 13.79 0 100
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N) \¡ \2E 72 20 E B c D' E 00 0 15
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46. 15 76.92 0 20.51 14.83 2i,92 53
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ECTODERM DISCONTINUITY IN EXPERIMEN
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279 ECTODERM DISCONTINUITY IN EXPER
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SOMITE SEPARATION IN EXPERIMENTAL E
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283 NOTOCHORD SEPARATION IN EXPERIM
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285 SOMITE DEFECTS IN EXPERIMENTAL
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287 and distr¡bfrtíon in the cont
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19.09 r8.95 r 1.84 14.82 15.20 0 17
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0 15. 89 81 .08 100 100 ' 76.92 0 1
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43. rB 100 100 0 12.53 74.07 r00 't
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7.t6 16.03 100 100 160 7.90 18.22 r
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Figs. 120'123. Percentage ie.ngths
Page 328 and 329:
299 O\TERLAP ZONE IN EXPERIMENTAL E
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301 OVERLAP ZONE IN EXPERIMENTAL EM
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303 ând every tenth sectlon was ne
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30c 12 16 c 17707,61 2463.3\ 7.19 D
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Ratio NT/N 4 .90 4.11 6.17 7.14 6.9
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Rêtlo NT/N 4.go \.36 3 .44 3. 18 3
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6.7t 6.lt 4.63 4.60 4.13 3.48 hzE 5
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Fi9s, 124-127, Neurál tube-norocho
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315 NEURAL TUBE -NOTOCHORD RATIOS I
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317 NEURAL TUBE-NOTOCHORD RATIOS IN
Page 348 and 349:
319 TABLE 598 ' ANALYSIS OF VARIANC
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321 TABLE 61., .NEURAL TISSUE/NOTOC
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323 Apart f.rom the sîgnîficant d
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t25 7. Dlscusst0N 1'/i th progressi
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327 C¡osure of the anterior neurop
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329 the mid-polnts of the defects w
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331 'c¡osure of the neural folds w
Page 362 and 363:
333 . These findings s.ugges r that
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335 Lendon (1968, 1975) and notos (
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337 Ferm, 1965; l"larin-Padi r ¡a,
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339 Kôplan (1965) and Kaplan and G
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341 reach the floor-plate; asymmetr
Page 372 and 373:
343 took up the label, shovri.ng th
Page 374 and 375:
345 The defects in early human embr
Page 376 and 377:
347 after pred¡cted closure (Lemî
Page 378 and 379:
349 hours could provide evidence fo
Page 380 and 381:
351 t971), Gal lus and Xenopus (l'l
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353 1962i 1965). Barth and Barth.(1
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The result of any teratogen¡c insu
Page 386 and 387:
357 Uindowîlg at ear¡y stages of
Page 388 and 389:
SUHHARY AND CONCLUS I ONS
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361 separatlon between the neural p
Page 392 and 393:
363 APPENDIX A Preparatlon of Early
Page 394 and 395:
365 APPENDIX B Stainl.ng of Carti l
Page 396 and 397:
367 10, BIBLIOGRAPHY, Alter, l.,l.
Page 398 and 399:
369 Braun, l'{. (1882). entwicklung
Page 400 and 401:
371 Crlley, B,B.(1969). Analysîs o
Page 402 and 403:
373 dqs anomal ies de lrorganizatio
Page 404 and 405:
375 Heath, H.D., Shear, H.H., lm€
Page 406 and 407:
377 Jel inek, R. (1960). Developmen
Page 408 and 409:
379 Laurence, K.14. (1964). Thé na
Page 410 and 411:
381 McKeown, T. and Record, R.G.(19
Page 412 and 413:
Penrose, L. S.(1957). Genetics of a
Page 414 and 415:
385 Russell, H.E. and A¡ tken' G.T
Page 416 and 417:
387 Spemann, H. (1938). Embryonic D
Page 418 and 419:
389 lJeed, ¡.H. (1937 -38'). M.nin
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