Focal dermal hypoplasia syndrome in a male

Clinical Genetics

Volumn 7, Issue 4, 1975, Pages 325-327

  Toro‐Sola, Maria A ^a   Kistenmacher, Mildred L ^a   Punnett, Hope H ^a   DiGeorge, Angelo M ^a  

^a ST CHRISTOPHER'S HOSPITAL FOR CHILDREN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADIPOCYTE; CONNECTIVE TISSUE; DENTITION; DIAGNOSIS; GOLTZ SYNDROME; HEMANGIOFIBROMA; HISTOLOGY; HYPOPIGMENTATION; MAJOR CLINICAL STUDY; MICROCEPHALY; PAPILLOMA; PIGMENTATION; PROMINENT EAR; SCALP HAIR; SCOLIOSIS; SEX DIFFERENCE; SHORT STATURE; SKIN HYPOPLASIA; TELANGIECTASIA; UPPER LIP; VERRUCA VULGARIS;

ABNORMALITIES, MULTIPLE; ATROPHY; CHILD; HUMAN; MALE; PIGMENTATION DISORDERS; SKIN DISEASES; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0016738841     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1975.tb00336.x     Document Type: Article

References (3)

1. Focal dermal hypoplasia syndrome. A review of the literature and report of two cases
2. Focal dermal hypoplasia
3. Focal dermal hypoplasia syndrome