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Journal of the American Academy of Dermatology

Volumn 16, Issue 4, 1987, Pages 899-906

Lethal genes surviving by mosaicism: A possible explanation for sporadic birth defects involving the skin

(1) Happle, Rudolf a

a UNIVERSITY OF MÜNSTER (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALBRIGHT SYNDROME; ANGIOOSTEOHYPERTROPHY SYNDROME; ARTICLE; CONGENITAL SKIN DISEASE; FEMALE; GENETICS; HEMANGIOMATOSIS; HUMAN; LETHAL GENE; MALE; MOSAICISM; MULTIPLE MALFORMATION SYNDROME; NEWBORN; PIGMENT DISORDER; SYNDROME;

ABNORMALITIES, MULTIPLE; ANGIOMATOSIS; FEMALE; FIBROUS DYSPLASIA, POLYOSTOTIC; GENES, LETHAL; HUMANS; INFANT, NEWBORN; KLIPPEL-TRENAUNAY-WEBER SYNDROME; MALE; MOSAICISM; PIGMENTATION DISORDERS; SKIN ABNORMALITIES; SYNDROME;

EID: 0023319298 PISSN: 01909622 EISSN: None Source Type: Journal
DOI: 10.1016/S0190-9622(87)80249-9 Document Type: Article

Times cited : (468)

References (39)

1
- 0015800876
- Linear nevus sebaceous [sic] syndrome: Report of two cases and a review of the literature
- (1973) Pediatrics , vol.52 , pp. 382-387
- Lovejoy, F¹ Boyle, WE²

2
- 0022611906
- Cutaneous manifestation of lethal genes
- (1986) Hum Genet , vol.72 , pp. 280
- Happle, R¹

3
- 0016798511
- Half chromatid mutations: Transmission in humans?
- (1975) Am J Hum Genet , vol.27 , pp. 218-223
- Gartler, SM¹ Francke, U²

4
- 0016548130
- Half chromatid mutations may explain incontinentia pigmenti in males
- (1975) Am J Hum Genet , vol.27 , pp. 690
- Lenz, W¹

5
- 0022654257
- The McCune-Albright syndrome: A lethal gene surviving by mosaicism
- (1986) Clin Genet , vol.29 , pp. 321-324
- Happle, R¹

6
- 0003802554
- Braumüller, Wien-Leipzig
- (1901) Die Nervenverteilung in der Haut in ihrer Beziehung zu den Erkrankungen der Haut
- Blaschko, A¹

7
- 0022416999
- Lyonization and the lines of Blaschko
- (1985) Hum Genet , vol.70 , pp. 200-206
- Happle, R¹

8
- 0016255314
- Zur Kenntnis des Schimmelpenning-Feuerstein-Mims-Syndroms (Organoide Naevus-Phakomatose)
- (1974) Arch Dermatol Forsch , vol.250 , pp. 35-50
- Hornstein, OP¹ Knickenberg, M²

9
- 85025534356
- ed. 6, Johns Hopkins University Press, Baltimore
- (1983) Mendelian inheritance in man: Catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes , pp. 320
- McKusick, VA¹

10
- 85025523707
- ed. 6, Johns Hopkins University Press, Baltimore
- (1983) Mendelian inheritance in man: Catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes , pp. 380

11
- 85025530222
- ed. 6, Johns Hopkins University Press, Baltimore
- (1983) Mendelian inheritance in man: Catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes , pp. 385

12
- 0013455952
- ed. 6, Johns Hopkins University Press, Baltimore
- (1983) Mendelian inheritance in man: Catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes , pp. 440

13
- 85025518465
- ed. 6, Johns Hopkins University Press, Baltimore
- (1983) Mendelian inheritance in man: Catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes , pp. 498

14
- 85025520088
- ed. 6, Johns Hopkins University Press, Baltimore
- (1983) Mendelian inheritance in man: Catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes , pp. 815

15
- 0021810129
- Neuroradiological findings in Jadassohn nevus phakomatosis: A report of four cases
- (1985) Eur J Pediatr , vol.144 , pp. 290-294
- Vles, JSH¹ Degraeuwe, P² De Cock, P³ Casaer, P⁴

16
- 0016577757
- Epidermal and other congenital organoid nevi
- (1975) Curr Probl Pediatr , vol.6 , pp. 3-56
- Solomon, LM¹ Esterly, NB²

17
- 0017797858
- McCune-Albright syndrome in a male child: A clinical and endocrinologic enigma
- (1978) J Pediatr , vol.92 , pp. 220-226
- Giovannelli, G¹ Bernasconi, S² Banchini, G³

18
- 0019814803
- Signes dermatologiques du syndrome de McCune-Albright: A propos d'un cas
- (1981) Ann Dermatol Venereol , vol.108 , pp. 969-976
- Pierini, AM¹ Ortonne, JP² Floret, D³

19
- 0017704884
- Fibrous dysplasia of bone: Report of female monozygotie twins with and without the McCune-Albright syndrome
- (1977) J Pediatr , vol.91 , pp. 947-949
- Lemli, L¹

20
- 0020534650
- The Proteus syndrome: Partial gigantism of the hands and/or feet, nevi, hemihypertrophy, subcutaneous tumors, macrocephaly or other skull anomalies and possible accelerated growth and visceral affections
- (1983) Eur J Pediatr , vol.140 , pp. 5-12
- Wiedemann, HR¹ Burgio, GR² Aldenhoff, P³

21
- 0021524827
- Further and new details on the Proteus syndrome
- (1984) Eur J Pediatr , vol.143 , pp. 71-73
- Burgio, GR¹ Wiedemann, HR²

22
- 0021962526
- Variability in the Proteus syndrome: Report of an affected child with progressive lipomatosis
- (1985) Eur J Pediatr , vol.143 , pp. 320-323
- Mücke, J¹ Willgerodt, H² Kiinzel, R³ Broek, D⁴

23
- 0019422320
- Orbital cyst in addition to congenital cerebral and focal dermal malformations: A new entity?
- (1981) Clin Genet , vol.19 , pp. 191-198
- Delleman, JW¹ Oorthuys, JWE²

24
- 0021259420
- Orbital cyst in addition to congenital cerebral and focal dermal malformations: A new entity
- (1984) Clin Genet , vol.25 , pp. 470-472
- Delleman, JW¹ Oorthuys, JWE² Bleeker-Wagemakers, EM³

25
- 0021275453
- Ocular, cerebral and cutaneous malformations: Confirmation of an association
- (1984) Clin Genet , vol.25 , pp. 464-469
- Ferguson, JW¹ Hutchison, HT² Rouse, BM³

26
- 0021952205
- Oculocerebrocutaneous syndrome
- (1985) Am J Ophthalmol , vol.99 , pp. 142-148
- Wilson, RD¹ Traverse, L² Hall, JG³

27
- 0039697483
- Klippel-Trenaunay syndrome
- PJ Vinken, GW Bruyn, North Holland Publishing Co., Amsterdam
- (1972) The phakomatoses: Handbook of clinical neurology , vol.14 , pp. 390-404
- Kramer, W¹

28
- 0003868876
- ed. 2, McGraw-Hill Book Co., New York
- (1976) Syndromes of the head and neck , pp. 412-417
- Gorlin, RJ¹ Pindborg, JJ² Cohen, MM³

29
- 33847696711
- Syndrome de Klippel-Trenaunay avec colobome irien atypique
- (1956) J Genet Hum , vol.5 , pp. 1-8
- Schnyder, UW¹ Landolt, E² Martz, G³

30
- 0014913455
- Sturge-Weber and Klippel-Trenaunay syndrome with nevus of Ota and Ito
- (1970) Arch Dermatol , vol.102 , pp. 640-645
- Furukawa, T¹ Igata, A² Toyokura, Y³ Ikeda, S⁴

31
- 0015068748
- Sturge-Weber syndrome with Klippel-Trenaunay-Weber syndrome
- (1971) Birth Defects , vol.7 , Issue.8 , pp. 314
- Harper, PS¹

32
- 0000284615
- The Klippel-Trenaunay syndrome: Varicosity, hypertrophy and hemangioma with no arteriovenous fistula
- (1965) Ann Surg , vol.162 , pp. 303-314
- Lindenauer, SM¹

33
- 0008155384
- Sturge-Weber syndrome
- PJ Vinken, GW Bruyn, North Holland Publishing Co., Amsterdam
- (1972) The phakomatoses: Handbook of clinical neurology , vol.14 , pp. 223-240
- Alexander, GL¹

34
- 25144506353
- Konkordanter doppelseitiger Trigeminusnaevus bei eineiigen Zwillingen nit gleiehartigen elektroenzephalographischen Befunden
- (1953) Dermatol Wschrift , vol.127 , pp. 488-493
- Teller, H¹ Lindner, B² Götze, W³

35
- 0018523994
- Przypadek dziedziczenia zespołu Sturge'a-Webera
- (1979) Klin Oczna , vol.81 , pp. 541-542
- Debicka, A¹ Adamczak, P²

36
- 76549183090
- Giant pigmented nevi, melanoma, and leptomeningeal melanocytosis. A clinical and histopathological study
- (1965) Arch Dermatol , vol.91 , pp. 100-119
- Reed, WB¹ Becker, SW² Becker, SW³ Nickel, WR⁴

37
- 0020043033
- Giant pigmented nevus occurring in one identical twin
- (1982) Arch Dermatol , vol.118 , pp. 188-189
- Amir, J¹ Metzker, A² Nitzan, M³

38
- 77049145238
- Bullous congenital ichthyosiform erythroderma
- (1953) Arch Dermatol Syph , vol.67 , pp. 443-455
- Barker, LP¹ Saehs, W²

39
- 0017834377
- Rescue of a lethal T/t locus genotype by chimaerism with normal embryos
- (1978) Nature , vol.272 , pp. 539
- Bennett, D¹

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