Birth Defects Original Article Series, Volume 15, Issue 1; Volume 18, Issue 5

Front Cover
A. R. Liss, 1965 - Abnormalities, Human - 281 pages

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
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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
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