Molecular cytogenetic analysis of a Xp21.3-pter deletion in a family with normal and short stature [2]

Clinical Genetics

Volumn 61, Issue 2, 2002, Pages 163-165

  Tachdjian, Gérard ^a   Perreaux, F ^b   Aboura, A ^b   Chevalier, P ^b   Portnoi, M F ^b   Esteva, B ^b   Trioche, P ^b   Labrune, P ^b  

^a HÔPITAL ANTOINE BÉCLÈRE   (France)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

GROWTH HORMONE;

BLOOD EXAMINATION; BODY BUILD; CASE REPORT; CHROMOSOME ANALYSIS; CHROMOSOME ARM; CHROMOSOME XP; CLINICAL FEATURE; ECHOGRAPHY; FEMALE; GENE DELETION; GROWTH RETARDATION; HEREDITY; HOMEOBOX; HORMONAL THERAPY; HUMAN; LABORATORY TEST; LETTER; LONG TERM CARE; MONOSOMY; PHYSICAL EXAMINATION; PRESCHOOL CHILD; PRIORITY JOURNAL; SHORT STATURE; TURNER SYNDROME; X CHROMOSOME;

BODY HEIGHT; BONE DEVELOPMENT; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; FAMILY HEALTH; FEMALE; GENE DELETION; GROWTH DISORDERS; HUMANS; KARYOTYPING; PHENOTYPE; X CHROMOSOME;

EID: 0036488076     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2002.610214.x     Document Type: Letter

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