| P2093 | author name string | Landau M | |
| | Krafchik BR | |
| P2860 | cites work | Watson syndrome: is it a subtype of type 1 neurofibromatosis? | Q24515021 |
| | Cowden's disease. A possible new symptom complex with multiple system involvement | Q28189705 |
| | Multiple Lentigenes Syndrome | Q28255802 |
| | Partial unilateral lentiginosis | Q71176680 |
| | Bloom's syndrome XI. Progress report for 1983 | Q71294647 |
| | The cutaneous features of tuberous sclerosis: a population study | Q71452977 |
| | Partial unilateral lentiginosis in a black patient with sickle cell anemia | Q71741728 |
| | Fanconi anemia | Q72146633 |
| | "Sunburn" freckles, café-au-lait macules, and other pigmented lesions of schoolchildren: the Vancouver Mole Study | Q72645929 |
| | Agminated lentiginosis: case report and review of the literature | Q72833880 |
| | Diagnostic importance of café-au-lait spot in neurofibromatosis | Q73148682 |
| | Familial occurrence of tuberous sclerosis | Q75713765 |
| | The prevalence of café-au-lait patches in tuberous sclerosis | Q93683006 |
| | Melanotic macules in Albright's syndrome and in neurofibromatosis | Q93770487 |
| | A new chromosomal instability disorder: the Nijmegen breakage syndrome | Q28281429 |
| | Noonan syndrome with café‐au‐lait spots and multiple lentigines syndrome are not linked to the neurofibromatosis type 1 locus | Q28291223 |
| | Syndrome Characterized by Osteitis Fibrosa Disseminata, Areas of Pigmentation and Endocrine Dysfunction, with Precocious Puberty in Females | Q29543750 |
| | Serum-alpha-fetoprotein levels in patients with ataxia-telangiectasia | Q34202283 |
| | Multiple non-ossifying fibromata with extraskeletal anomalies: a new syndrome? | Q34265262 |
| | The incidence and significance of birthmarks in a cohort of 4,641 newborns | Q34266047 |
| | Diagnostic and genetical aspects of tuberous sclerosis | Q34633125 |
| | Café-au-lait spots in schoolchildren | Q35116220 |
| | Ataxia-telangiectasia. Report of a case and review of the literature | Q35319140 |
| | The Silver-Russel syndrome: a case with sexual ambiguity, and a review of literature | Q35902419 |
| | Diagnostic value of the café-au-lait spot in children | Q36061096 |
| | Pulmonary stenosis, cafe-au-lait spots, and dull intelligence | Q36061485 |
| | Two patients with ring chromosome 15 syndrome | Q37372185 |
| | Frequency of congenital nevi, nevi spili and café-au-lait spots and their relation to nevus count and skin complexion in 939 children. | Q37923854 |
| | Familial glioblastoma with hepatic focal nodular hyperplasia | Q40001069 |
| | Von Recklinghausen neurofibromatosis | Q40262766 |
| | Neurofibromatosis: clinical heterogeneity | Q40266828 |
| | Severe endocrine and nonendocrine manifestations of the McCune-Albright syndrome associated with activating mutations of stimulatory G protein GS. | Q40864479 |
| | Cutaneous findings in ring chromosome 7 syndrome | Q40872967 |
| | Molecular genetics of Bloom's syndrome | Q41170320 |
| | Noonan's syndrome and neurofibromatosis | Q41767343 |
| | Hereditary congenital hypopigmented and hyperpigmented macules | Q41775021 |
| | Ring chromosome 11 and café-au-lait spots | Q41932306 |
| | The eastern Australian childhood nevus study: prevalence of atypical nevi, congenital nevus-like nevi, and other pigmented lesions | Q44018043 |
| | McCune-Albright Syndrome with Multiple Bilateral Cafe au Lait Spots | Q44082568 |
| | Macrocephaly, multiple lipomas, and hemangiomata (Bannayan-Zonana syndrome): genetic heterogeneity or autosomal dominant locus with at least two different allelic forms? | Q45261185 |
| | The number and distribution of benign pigmented moles (melanocytic naevi) in a healthy British population | Q49246214 |
| | The incidence of birthmarks in Israeli neonates. | Q51046943 |
| | Ring chromosome 12 | Q52071213 |
| | The nature and origin of the melanin macroglobule. | Q52273413 |
| | The giant melanosome: a model of deranged melanosome-morphogenesis. | Q53702083 |
| | Ultrastructure of giant pigment granules (macromelanosomes) in the cutaneous pigmented macules of neurofibromatosis. | Q53891290 |
| | Familial Multiple Cafe au lait Spots | Q56502683 |
| | The syndrome of congenital telangiectaticerythema and stunted growth | Q57462560 |
| | Melanotic macules following Blaschko's lines in McCune-Albright syndrome | Q57733151 |
| | The McCune-Albright syndrome: a lethal gene surviving by mosaicism | Q59540943 |
| | The Hunt for the Neurofibromatosis Gene | Q59666899 |
| | Primary osteoma cutis — multiple café-au-lait spots and woolly hair anomaly | Q59829204 |
| | Common and uncommon cutaneous findings in patients with ataxia-telangiectasia. | Q64901621 |
| | Unusual cutaneous manifestations of anhidrotic ectodermal dysplasia--a case report | Q68884176 |
| | Multiple Hamartoma Syndrome (Cowden's Disease) | Q69386355 |
| | Bloom's syndrome | Q69400681 |
| | The Cowden syndrome: a clinical and genetic study in 21 patients | Q69486172 |
| | Congenital-nevus-like nevi, nevi spili, and café-au-lait spots in patients with malignant melanoma | Q70061324 |
| | The phenomenon of halo-like disappearance of the Mongolian spot on lesions combined with café au lait spot or acquired pigmented nevus | Q70190113 |
| | Gastro-cutaneous syndrome: peptic ulcer/hiatal hernia, multiple lentigines/café-au-lait spots, hypertelorism, and myopia | Q70301749 |
| | Ataxia-telangiectasia | Q70392723 |
| | Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: evidence of non-linkage | Q70620389 |
| P433 | issue | 6 Pt 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 877-90; quiz 891-2 | |
| P577 | publication date | 1999-06-01 | |
| P1433 | published in | Journal of the American Academy of Dermatology | Q15757046 |
| P1476 | title | The diagnostic value of café-au-lait macules | |
| P478 | volume | 40 | |