Birth Defects Original Article Series, Volume 15, Issue 1; Volume 18, Issue 5 |
Contents
145 | 47 |
120 | 47 |
133 | 47 |
125 | 48 |
17 | 49 |
7 | 50 |
164 | 51 |
168 | 53 |
8 | 249 |
315 | 250 |
YCongenital ichthyosis oligophrenia and spastic paresis Sjögren Larsson syndrome | 251 |
140 | 252 |
Authors Index 253 Index | 253 |
The Fsyndrome | 254 |
QAcrokeratosis verruciforms | 255 |
Recent Advances in Human Genetics | 256 |
54 Tables of Contents | 55 |
45 | 56 |
185 | 57 |
27 | 58 |
173 | 59 |
285 | 61 |
64 Tables of Contents | 66 |
18 Tables of Contents | 70 |
190 | 71 |
20 Tables of Contents | 72 |
800 | 74 |
207 | 78 |
153 | 80 |
112 | 82 |
24 Tables of Contents | 83 |
12 Tables of Contents | 84 |
114 | 85 |
105 | 87 |
137 | 89 |
Tables of Contents | 90 |
219 | 91 |
familial presentation | 92 |
309 | 93 |
215 | 95 |
322 | 97 |
Tables of Contents | 99 |
fetus | 100 |
137 | 101 |
139 | 102 |
185 | 104 |
295 | 105 |
199 | 109 |
36 Tables of Contents | 112 |
52 | 113 |
218 | 114 |
298 | 115 |
418 | 117 |
Tables of Contents | 118 |
508 | 119 |
14 Tables of Contents | 120 |
207 | 121 |
324 | 122 |
8 | 125 |
209 | 127 |
Drugs and the intrauterine patient Jerold F Lucey | 129 |
221 | 130 |
Catherine A Neill Richard D | 133 |
23 | 135 |
5 | 136 |
117 | 139 |
305 | 141 |
The placental barrier and infections of the fetus Heinz Eichenwald | 142 |
Jay Bern | 144 |
18 | 146 |
267 | 147 |
211 | 148 |
mationsW P Kennedy | 150 |
10 | 152 |
20 | 153 |
319 | 155 |
The nosology of extrapyramidal disorders Andre Barbeau | 156 |
11 | 158 |
138 | 159 |
8 | 160 |
introduction | 161 |
Subject Index | 163 |
18 | 164 |
40 | 165 |
226 | 166 |
Heterogeneity in osteogenesis imperfecta Kenneth H Ibsen | 167 |
424 | 168 |
28 | 169 |
194 | 170 |
274 | 171 |
64 | 172 |
51 | 173 |
443 | 175 |
66 | 176 |
71 | 177 |
Dominant olivopontocerebellar atrophy with dementia and extrapyra midal signs Report of a family through three generations Bruce W Konigsmark ... | 178 |
333 | 179 |
ALattice degeneration of the cornea | 180 |
56 | 181 |
251 | 182 |
106 | 183 |
82 | 184 |
459 | 186 |
542 | 187 |
286 | 188 |
586 | 189 |
123 | 190 |
116 | 191 |
Hereditary disease of the cerebellar parenchyma Leslie P Weiner Bruce W Konigsmark | 192 |
310 | 193 |
228 | 194 |
237 | 195 |
129 | 196 |
128 | 197 |
14 | 198 |
343 | 200 |
241 | 203 |
48 | 204 |
15 | 205 |
Case Reports | 206 |
73 | 207 |
318 | 208 |
231 | 209 |
The disappearance of calcified tissue Jenifer Jowsey | 210 |
20 | 211 |
Section IVFunctional Deficiencies in Agammaglobulinemia | 212 |
James G White Robert A Good | 213 |
a recessively inherited form of presenile dementia with motor disturbances | 214 |
346 | 215 |
E Two distinct types of autosomal dominant spastic paraplegia | 216 |
46 | 217 |
283 | 218 |
FTwo kindreds with a sexlinked recessive form of spastic paraplegia | 219 |
99 | 220 |
GJuvenile amyotrophic lateral sclerosis in two brothers from an in bred community | 222 |
74 | 223 |
143 | 224 |
301 | 225 |
11 | 226 |
148 | 227 |
JFamilial megalencephaly | 228 |
82 | 229 |
98 | 230 |
KFamilial hydrocephalus | 231 |
42 | 232 |
155 | 233 |
MArnoldChiari malformation in sibs | 234 |
316 | 235 |
298 | 236 |
ORefsums disease heredopathia atactica polyneuriformis | 238 |
171 | 239 |
204 | 240 |
166 | 241 |
Section VIGenetic Considerations in Immunologic Deficiency | 242 |
113 | 243 |
77 | 244 |
179 | 245 |
TOlivopontocerebellar degeneration with macular dystrophy 246 UCerebellar ataxia | 246 |
92 | 247 |
WRoussyLevy hereditary areflexic dystasia | 248 |
49 | 257 |
165 | 261 |
UChediakHigashi syndrome in brothers | 262 |
126 | 263 |
MEngelmanns disease a form of craniodiaphyseal dysplasia | 264 |
CSexual ateleiotic dwarfism associated with normal plasma growth | 265 |
Visceral anomalies in an infant with the Goldenhar syndrome | 268 |
150 | 269 |
YNevus sebaceus of Jadassohn with associated syringocystadeno | 270 |
Autosomal dominant inheritance of shortening of the flexor profundus | 271 |
328 | 275 |
178 | 277 |
The aniridiaWilms tumor syndrome | 278 |
166 | 279 |
IFacial cleft | 281 |
EEHaileyHailey disease chronic benign familial pemphigus | 283 |
BBThe floppy mitral valve syndrome | 284 |
C3317 Hydroxylation deficiency with mineralocorticoid | 285 |
JFacial cleft facial hemiatrophy and congenital heart disease | 287 |
183 | 288 |
FFAortic and mitral valve involvement in osteogenesis imperfecta | 290 |
Animal models in the clinical study of birth defects in man Mark V | 291 |
113 | 292 |
JJHemifacial atrophy the Romberg syndrome | 293 |
172 | 295 |
Genetically determined unconjugated hyperbilirubinemia Lawrence | 296 |
340 | 298 |
120 | 299 |
NNEhlersDanlos Syndrome | 300 |
179 | 301 |
NNXanthoma and hypercholesterolemia in a Mennonite family | 302 |
PPThe stiff skin syndrome | 306 |
138 | 308 |
204 | 310 |
185 | 311 |
TTSturgeWeber syndrome encephalofacial angiomatosis | 312 |
EFocal dermal hypoplasia Goltz syndrome | 316 |
223 | 317 |
two cases in unre | 318 |
congenital heart disease | 319 |
174 | 320 |
357 | 321 |
188 | 323 |
229 | 328 |
208 | 329 |
191 | 331 |
tower skull | 334 |
215 | 340 |
Genetic heterogeneity in antihemophilic globulin deficiency Jack | 347 |
UIncomplete testicular feminization | 350 |
220 | 351 |
DPfeiffer syndrome | 353 |
370 | 355 |
an inbred group | 356 |
36 | 358 |
E Pseudoachondroplastic dysplasia | 362 |
651 | 363 |
fatal intrahepatic cholestasis Louie G Linarelli C | 364 |
G Type III pseudoachondroplastic dysplasia dominant inheritance | 368 |
224 | 371 |
H Spondyloepiphyseal dysplasiaunclassified type | 375 |
278 | 376 |
233 | 377 |
J Spondyloepiphyseal dysplasia tarda Xlinked form | 383 |
RLebers congenital amaurosis and mental retardation | 385 |
236 | 386 |
23 | 390 |
326 | 392 |
238 | 393 |
296 | 394 |
33 | 399 |
247 | 403 |
330 | 406 |
Studies of Acatalasemia | 410 |
64 | 412 |
299 | 414 |
David W Hollister Ralph S Lachman Robert L Kaufman William | 415 |
273 | 417 |
EMG syndrome | 418 |
Q Probable multiple epiphyseal dysplasia | 419 |
139 | 421 |
67 | 423 |
46 | 425 |
80 | 429 |
T Simultaneous parastremmatic dwarfism and osteogenesis imper | 430 |
69 | 432 |
334 | 437 |
91 | 438 |
RGenetic counseling in cystic fibrosis | 439 |
83 | 440 |
303 | 442 |
W Shortlimbed dwarfismpossibly metaphyseal chondrodys | 445 |
220 | 446 |
100 | 451 |
35 | 452 |
357 | 453 |
77 | 455 |
195 | 456 |
48 | 459 |
3 | 460 |
225 | 461 |
373 | 464 |
Z The Morquio Syndrome MPS | 465 |
52 | 467 |
51 | 468 |
131 | 470 |
383 | 473 |
65 | 474 |
63 | 480 |
Index | 484 |
FF The Coffin syndrome | 491 |
24 | 493 |
706 | 497 |
72 | 499 |
Rickets and osteomalacia of various origins Charles E Dent | 500 |
93 | 505 |
T SE 2 8 5 52 | 508 |
NLow birth weight dwarfism in two brothers | 509 |
Author Index | 515 |
White Walter E Nance Charles E Jackson Susan Desnick | 516 |
Characterization of banding patterns of metaphaseprophase Gbanded | 517 |
Recent advances in human biochemical genetics H Hugh Fuden | 518 |
impact | 520 |
Congenital absence of the thymus and its immunologic conse | 527 |
Phenotypic aspects of sex chromosome aberrations | 531 |
Robert S Krooth | 534 |
Variations in the subclasses of IgG William D Terry | 535 |
Genetic craniotubular bone dysplasias and hyperostosisa critical | 539 |
Tcell deficiency in DiGeorge syndrome Harold W Lischner Dale | 540 |
Professional responsibility in prenatal genetic evaluation M Neil | 550 |
Morphologic approaches to the nosology of nervous system | 552 |
A note on some aspects of von Willebrand disease | 554 |
Discussion of osteopathia striata Hooshang Taybi Arnold | 556 |
52 | 558 |
Human factors in genetic counseling | 560 |
Coarctation of the aorta in the fetal and neonatal periods | 564 |
Androgeninsensitive male pseudohermaphroditism Jan E Jirįsek | 568 |
treatment of cultured skin | 570 |
An ethical analysis of responsible parenthood Sidney Callahan | 572 |
B group shortarm deletion syndromes Heddie O Sedano Richard | 576 |
The XYY syndromea genetic determinant of behavior J Philip | 577 |
the early presentation of the pheno | |
moin Arthur L Prensky William S | |
Copyright | |